CN111065282A

CN111065282A - Composition containing microparticle composite and method for producing same

Info

Publication number: CN111065282A
Application number: CN201880055905.5A
Authority: CN
Inventors: 樋口达也; 井原淳一郎
Original assignee: Mizkan Holdings Co Ltd
Current assignee: Mizkan Holdings Co Ltd
Priority date: 2018-04-06
Filing date: 2018-10-11
Publication date: 2020-04-24
Anticipated expiration: 2038-10-11
Also published as: TWI687168B; KR20200021541A; AU2018417768A1; CA3071083A1; CA3071083C; BR112020007094B1; EP3639679A4; AU2018417768B2; BR112020007094A2; PH12020500112A1; KR102207648B1; EP3639679A1; US11678686B2; CN111065282B; WO2019193780A1; AU2018417768C1; TW201943339A; SG11202000194SA; US20200187543A1

Abstract

One of the objects of the present invention is: the food containing insoluble dietary fiber has improved properties such as taste such as astringency and easy intake. A composition containing a microparticle complex comprising insoluble dietary fibers, which satisfies the following (1) to (5) and at the same time satisfies one or more of the following (6-1) to (6-3): (1) contains 0.1 mass% or more of insoluble dietary fiber; (2) the total oil content is less than 20 mass percent; (3) the maximum grain size before ultrasonic treatment is more than 100 mu m; (4) the mode diameter before ultrasonic treatment is 5-400 [ mu ] m; (5) the mode diameter after ultrasonic treatment is more than 0.3 μm and less than 100 μm; (6-1) the value N (I) obtained by the following formula (I) is 1.20Wherein (6-2) the numerical value N (II) obtained by the following formula (II) is 1.40 or more, (2) N (II) = (α/β)/ω (II), (6-3) the numerical value N (III) obtained by the following formula (III) is 0.50 or more, and (3) N (III) = (α/β) × γ_A(III)。

Description

Composition containing microparticle composite and method for producing same

Technical Field

The present invention relates to compositions comprising a microparticle complex comprising insoluble dietary fibers and methods of making the compositions.

Background

Conventionally, it has been desired that a composition containing dietary fibers having various active ingredients be positively ingested in accordance with the health function thereof. However, since a composition containing a large amount of dietary fiber is poorly formulated in other foods, it cannot be taken sufficiently by daily diet, and thus application to various uses is hindered.

As a composition containing only broken dietary fibers, for example, there are reported: a seasoning obtained by pulverizing a yellow-green vegetable in the presence of oil (patent document 1); or a spread obtained by pulverizing a non-nut plant material to obtain a powder having an average particle size of less than about 100 μm and then exposing the obtained powder to a high temperature (temperature rise) (patent document 2).

Further, as a technique for reducing aggregates generated during fine grinding of particles, there has been reported a method for producing a fine particle dispersion, in which an aggregated powder of fine particles is subjected to wet grinding, and grinding is performed while suppressing re-aggregation of the ground fine particles (patent document 3).

In addition, in particular, food products containing insoluble dietary fibers insoluble in water have astringency which is a great obstacle to daily intake.

As a technique for improving the astringency of foods, a method for producing a fruit jelly in which the astringency or bitterness derived from chitosan is suppressed by adding a calcium salt or a sulfate salt to improve the taste has been reported (patent document 4).

Documents of the prior art

Patent document

Patent document 1: japanese patent laid-open No. 2006-141291;

patent document 2: japanese patent laid-open publication No. 2009-543562;

patent document 3: japanese patent laid-open publication No. 2010-023001;

patent document 4: japanese patent laid-open No. 5-236888.

Disclosure of Invention

Problems to be solved by the invention

However, patent documents 1 and 2 are not satisfactory in terms of taste, particularly astringency, and ease of intake when applied to food products containing insoluble dietary fibers.

In addition, patent document 3 is a technique that cannot be applied to food because it uses a silane coupling agent as a dispersant.

Patent document 4 is effective for improving astringency derived from chitosan, but is a technique that cannot be applied to food products containing insoluble dietary fibers.

One of the objects of the present invention is: the food containing insoluble dietary fiber has improved properties such as taste such as astringency and easy intake.

Means for solving the problems

The inventors of the present invention have intensively studied and found that: by forming a complex which can be broken by external disturbance by micronizing insoluble dietary fibers and controlling the shape of the complex within a predetermined range, the properties of the insoluble dietary fibers such as astringency can be improved. In addition, it has been found that: the composition containing the microparticle complex of insoluble dietary fiber has various other preferable characteristics, and can be applied not only to foods but also to other uses.

Namely, the present invention provides the following inventions [1] to [27 ].

[1] A composition containing a microparticle complex comprising insoluble dietary fibers, which satisfies the following (1) to (5) and at the same time satisfies one or more of the following (6-1) to (6-3):

(1) contains 0.1 mass% or more of insoluble dietary fiber;

(2) the total oil content is less than 20 mass percent;

(3) the maximum grain size before ultrasonic treatment is more than 100 mu m;

(4) the mode diameter before ultrasonic treatment is 5-400 [ mu ] m;

(5) the mode diameter after ultrasonic treatment is more than 0.3 μm and less than 100 μm;

(6-1) the value N (I) obtained by the following formula (I) is 1.20 or more;

(math formula 1)

N(I)＝(α/β) (I)

(6-2) the value N (II) obtained by the following formula (II) is 1.40 or more;

(math figure 2)

N(II)＝(α/β)/ω (II)

(6-3) the value N (III) obtained by the following formula (III) is 0.50 or more;

(math figure 3)

N(III)＝(α/β)×γ_A(III)

Wherein, in the above formulas (I) to (III),

α represents a value of 90% of the "major axis" before ultrasonic treatment measured by a particle shape image analyzer,

β represents a value of 90% of the "minor axis" before ultrasonic treatment measured by a particle shape image analyzer,

ω represents a 10 percentile value of "unevenness" before ultrasonic treatment measured by a particle shape image analysis device,

γ_Athe specific surface area per unit volume after the ultrasonic treatment is shown.

[2] [1] the composition according to any one of the preceding claims, wherein the water content/(water content + total oil component content) is 75% or more.

[3][1]Or [2]]The composition of (a), wherein the specific surface area per unit volume (γ) before ultrasonic treatment_B) Specific surface area per unit volume (gamma) after ultrasonic treatment_A) Ratio of (gamma)_B/γ_A) Is 0.8 or less.

[4] The composition according to any one of [1] to [3], which has an emulsifying capacity of 50% or more.

[5] The composition according to any one of [1] to [4], wherein the content of the microparticle complex is 4% by mass or more and 98% by mass or less.

[6] The composition according to any one of [1] to [5], wherein the insoluble dietary fiber comprises dietary fiber derived from an edible part and/or an inedible part of a food material containing the insoluble dietary fiber.

[7] [6] the composition according to, wherein the insoluble dietary fiber comprises dietary fibers derived from an edible part and an inedible part of the same kind of food material containing insoluble dietary fiber.

[8] The composition according to [6] or [7], wherein the food material containing insoluble dietary fiber is one or more selected from seeds, grains, beans, vegetables and fruits.

[9] [8] the composition, wherein the food material containing insoluble dietary fiber is at least one material selected from carrot, pumpkin, corn, soybean, green soy bean, chili pepper, beet, green pea, broccoli and tomato.

[10] [9] the composition, wherein the non-edible part of the food material containing insoluble dietary fiber is at least one selected from the group consisting of a core of sweet corn, a seed or a pedicle of hot pepper, a seed or a flesh of pumpkin, a skin of beet, a stem and leaf of broccoli, a pod of green soybean, and a pedicle of tomato.

[11] The composition according to any one of [6] to [10], which comprises a pulverized product of a food material containing insoluble dietary fibers.

[12] [11] the composition according to any one of the above aspects, wherein the pulverization treatment product is a medium-stirring mill treatment product.

[13] [12] the composition according to any one of the above aspects, wherein the medium-agitation-mill-treated product is a wet-medium-agitation-mill-treated product.

[14] The composition according to any one of [11] to [13], which satisfies one or more of the following (6-1 ') to (6-3'):

(6-1') the grinding treatment is carried out until the value N (I) obtained by the formula (I) is increased by 5% or more before and after the grinding;

(6-2') the grinding treatment is carried out until the numerical value N (II) obtained by the formula (II) is increased by 5% or more before and after the grinding;

(6-3') the grinding treatment is carried out until the numerical value N (III) obtained by the above formula (III) is increased by 5% or more before and after the grinding.

[15] A food or drink (drink, beverage or food) comprising the composition according to any one of [1] to [14 ].

[16] A liquid seasoning comprising the composition according to any one of [1] to [14 ].

[17] A method for producing the composition according to any one of [1] to [14], the method comprising: the food material containing insoluble dietary fiber is pulverized.

[18] The method according to [16] or [17], wherein the pulverization treatment is a medium-stirring mill treatment.

[19] [18] the method according to any one of the above methods, wherein the pulverization treatment is a wet media agitation and milling treatment.

[20] The method according to any one of [17] to [19], wherein the media-agitating mill treatment is performed under a pressure condition in which a maximum pressure is 0.01MPa or more and 1MPa or less.

[21][17]～[20]The method of any one of, wherein the media agitation mill treatment is at a treatment temperature T at the start of the treatment₁(. degree. C.) and the treatment temperature at the end, T₂(DEG C) under a temperature-raising condition satisfying the following formula (A):

(math figure 4)

T₁+1＜T₂＜T₁+50 (A)

[22] The method according to any one of [17] to [21], wherein the water activity value of the insoluble dietary fiber-containing food material is 0.95 or less.

[23] The method according to any one of [17] to [22], wherein the amount of available carbohydrate in the insoluble dietary fiber-containing food material is 2% by mass or more.

[24] A method of increasing the emulsification capacity of a composition comprising insoluble dietary fiber, the method comprising: the composition according to any one of [1] to [14] is formed by subjecting a composition containing an insoluble dietary fiber to a pulverization treatment.

[25] A method of improving the astringency of a composition comprising insoluble dietary fiber, the method comprising: the composition according to any one of [1] to [14] is formed by subjecting a composition containing an insoluble dietary fiber to a pulverization treatment.

[26] A method for producing a liquid seasoning by using the composition according to any one of [1] to [14 ].

[27] [17] to [26], wherein the pulverization treatment is performed until one or more of the following (6-1 ') to (6-3') is satisfied:

(6-1') the value N (I) obtained by the above formula (I) is increased by 5% or more before and after pulverization;

(6-2') the value N (II) obtained by the above formula (II) is increased by 5% or more before and after pulverization;

(6-3') the numerical value N (III) obtained by the above formula (III) is increased by 5% or more before and after the pulverization.

Effects of the invention

The composition containing a microparticle complex of insoluble dietary fibers according to the present invention is excellent in taste improvement properties such as astringency derived from insoluble dietary fibers.

Detailed Description

The present invention is not limited to these embodiments, and can be carried out with any modification without departing from the gist thereof.

[ composition containing insoluble dietary fiber ]

One aspect of the invention relates to: a composition comprising a microparticle complex comprising insoluble dietary fibers (hereinafter appropriately referred to as "the composition of the present invention").

[ insoluble dietary fiber ]

The composition of the present invention contains insoluble dietary fiber. In the present invention, "dietary fiber" refers to the total of indigestible components in food products that are not digested by human digestive enzymes. In addition, in the present invention, "insoluble dietary fiber" means water-insoluble dietary fiber among dietary fibers. Examples of the insoluble dietary fiber include, but are not limited to: lignin, cellulose, hemicellulose, chitin, chitosan, etc. However, even in insoluble dietary fibers, the intake of lignin, particularly acid-soluble lignin, is significantly poor, and therefore the intake improving effect can be more significantly obtained by the application of the present invention. From this viewpoint, lignin, particularly acid-soluble lignin, is preferable as the insoluble dietary fiber.

The composition of the present invention contains insoluble dietary fiber at a content of not less than a certain level. Specifically, the lower limit of the content of the insoluble dietary fiber in the composition of the present invention is usually 0.1 mass% or more. Among them, it is preferably 0.2% by mass or more, more preferably 0.3% by mass or more, more preferably 0.4% by mass or more, more preferably 0.5% by mass or more, particularly preferably 0.7% by mass or more, or 1% by mass or more, or 1.5% by mass or more, or 2% by mass or more, particularly preferably 3% by mass or more. It is preferable to set the content of insoluble dietary fiber to the lower limit or more because "eating quality" of the composition is significantly improved. On the other hand, the upper limit of the content of the insoluble dietary fiber in the composition of the present invention is not limited, and is usually 20 mass% or less, preferably 15 mass% or less, and more preferably 10 mass% or less, from the viewpoint of industrial productivity.

The composition of the insoluble dietary fiber in the composition of the present invention is not limited. However, for the above reasons, when the ratio of lignin (acid-soluble lignin among them) in the whole insoluble dietary fiber is equal to or more than a certain value, the effect of improving the intake property can be more remarkably obtained by the application of the present invention. Specifically, the dry mass ratio of lignin (acid-soluble lignin in the lignin) to the whole insoluble dietary fiber is usually 5% or more, preferably 10% or more, and more preferably 30% or more.

The source of the insoluble dietary fiber is not limited, and may be a fiber derived from various natural materials containing insoluble dietary fiber or a fiber derived from a synthetic fiber. In the former case, insoluble dietary fibers contained in various materials may be separated and purified and used, or such insoluble dietary fiber-containing materials may be used as they are. In the latter case, as the material containing insoluble dietary fiber, a food material is preferable. The food material containing insoluble dietary fiber will be described later.

The Prosky method is an example of a method for determining dietary fiber and insoluble dietary fiber.

[ food Material containing insoluble dietary fiber ]

As described above, the insoluble food fiber contained in the composition of the present invention is preferably a fiber derived from food materials. Further, the composition of the present invention preferably comprises a food material containing insoluble dietary fiber. The type of the food material containing insoluble dietary fiber is not limited, and any food material may be used as long as it is suitable for a diet. However, it is preferable to contain the insoluble dietary fiber at a certain ratio or more. Specifically, the dry mass ratio of the insoluble dietary fiber to the food material is usually 1 mass% or more, preferably 3 mass% or more, more preferably 5 mass% or more, and particularly 10 mass% or more.

Examples of such food materials containing insoluble dietary fibers include: plant-based food materials, microbial-based food materials, animal-based food materials, and the like, but are not limited thereto. Among them, vegetable food materials are preferable. Examples of the vegetable food material include: vegetables (including taro, mushroom), fruits, spices, algae, grains, seeds, beans, etc., but not limited thereto. One of these food materials may be used, or two or more of these food materials may be used in combination. The food materials may be used as they are, or may be used after various treatments (for example, drying, heating, removing alkaline water, peeling, removing seeds, ripening, salting, and processing pericarp).

The vegetables may be any ones as long as they contain insoluble dietary fibers in the edible part and/or the non-edible part. By way of example, mention may be made of: radish, carrot, turnip cabbage, parsnip, turnip, black-peel polo ginseng, sweet potato, cassava, snow lotus potato, wild taro, konjac (Polynesian, arowoot)), lotus root, potato, purple sweet potato, Beet (Beets) (suitably Beet (Beets) (Beet root)): improved variety for eating beet root), jerusalem artichoke, arrowhead, green onion, garlic, allium macrostemon, lily, jaborandi (castanea sativa), kale, yam japanese, yam chinese, onion, asparagus, heracleum hemsleyanum michaux, cabbage, lettuce, spinach, cabbage, rape, pinus parviflora, green stem, leek, welsh onion, wild lycopus herb, coltsfoot, spinach (watercress, eruca sativa), nonaceae, tomato, eggplant, pumpkin, sweet pepper, cucumber, zingiber mioga, cauliflower, broccoli, edible chrysanthemum, bitter gourd, okra, artichoke, zucchini, Sugarbeet (sugarbeets), tiger nut, ginger, perilla, horseradish, capsicum, spice plants (watercress, coriander, swamp cabbage, celery, chrysanthemum indicum, chive, thin leaf parsley, sage, thyme, bay, parsley, green (murd, green), Mustard green, eagle, Mustard green, targe, celery, cabbage, black sesame, black, Basil, oregano, rosemary, peppermint, savory, lemon grass, dill, horseradish leaf, zanthoxylum bungeanum leaf, stevia, bracken, osmunda japonica, kudzuvine, tea tree (tea), bamboo shoot, mushroom, tricholoma matsutake, agaric, shiitake mushroom, polypore, oyster mushroom, pleurotus eryngii, flammulina velutipes, pleurotus cornucopiae, armillaria mellea, agaricus blazei, nameko mushroom, suillus lactiflora (zech cow mushroom), russula vinosa, stropharia lactiflora, etc. Among them, carrot, pumpkin, tomato, capsicum, cabbage, Beet (Beet) (preferably Beet (Beets) (beetroot))), onion, broccoli, asparagus, purple sweet potato, and the like are preferable, and carrot, pumpkin, tomato, capsicum, Beet (Beet) (preferably Beet (beetroot) (beetroot))), broccoli, and the like are particularly preferable, but not limited thereto.

The fruit may be any fruit as long as it contains insoluble dietary fiber in the edible part and/or the inedible part. By way of example, mention may be made of: the fruit of the Mulberry tree (mulbery, Mulberry), cranberry (bergamot), pyrus betulaefolia (Shipova), apple, american cherry (Black cherry), Black cherry (dark cherry), Apricot fruit (Apricot ), plum (plum), cherry (cherry), sweet cherry, prunus cerasus, prunus nigra, plum (plum, nectarine), peach, ginkgo, chestnut, ricepaperplant (akebia), fig (fig), persimmon, blackcurrant (blackcurrant), raspberry (raspberry), kiwi fruit (kiwi), elaeagnus punica, prunus japonica, prunus dulcis (prunus dulcis), prunus punica, prunus dulcis (prunus punica, prunus, cornus), fruit of Mulberry, cranberry (cranberry), blueberry, bergenia, kochia, prunus, pru, Sea buckthorn (seabuckthorn)), black currant (Ribes sinannense), black currant (Gooseberry)), jujube (jujube), prune (Tibet, plum, bush), Lonicera caerulea (Lonicera caerulea), Morus alba (Bilberry), red currant (Ribes rubrum), Rubus idaeus (Red currant)), Grape (Grape), blackberry, blueberry, papaya (papaya, guava, Piper nigrum), Schisandra chinensis, raspberry (raspberry), prunus hypoglauca (Prunus), tangerine, trifoliate orange, olive, Loquat (Loquat), waxberry (ヤマモモ) (prunus davurica, Myrica rubra), Momordica grosvenorii, tropical fruits (mango, mangosteen, papaya, Peru's apple, litchi, Annona custara, banana, durian, caramonus guava, watermelon, passionfruit, apple, etc.), tropical fruits (papaya, melon, strawberry, etc, Avocado, miracle fruit, orange, lemon, prune, grapefruit, tangerine, grapefruit, lime, Taiwan fragrant lemon, etc. Among them, avocado, apple and the like are preferable, but not limited thereto.

The algae may be any algae as long as they contain insoluble dietary fibers in the edible part and/or the inedible part. By way of example, mention may be made of: macroalgae such as sea tangle, wakame seaweed, sea moss, Enteromorpha, and Eucheuma Gelatinosum; or microalgae such as green algae, red algae, blue algae, dinoflagellates, and euglena, but not limited thereto. As specific examples, there may be mentioned: ulva lactuca, Enteromorpha (green seaweed), Ulva pertusa, Vitis amurensis (caulerpa lentillifera), Cladophora elongata, Vitis vinifera, Pinctada cylindra, Pinctada glomerata, Ascophyllum nodosum (sea lily), Monostroma nitidum, Enteromorpha compressa, Pteridium crassa, Enteromorpha crassa, Ceratophyllum distichum, Echinotus, Scotus japonicus, Codium costatum, Costus lanceolatus, Ascophyllum arborescens, Ascophyllum nodosum, Cladosiphonium okamurense, Synechocystis, Pychnophora, Hemerocallis, Pyctolaginoidea (Pyropipia tenuipidula), Dictyota reticulum, Ecklonia cava (crude cloth), Hemerocallis fulva, Hemerocallis (Hemerocallis), Phaeophytes latina, Sargassum macrocephalum, Undariellana, Undaria, Undariffa pinnatifida, Euglena lancifolia, Laminaria stolonifera, Euglena lania latifolia, Eu, Laminaria religiosa), Chrysophytum, Cinnamomum mairei (Hemerocallis), Verbena columni, Nemacystus decipiens (clound), Chondrichthys crassifolia, Undaria pinnatifida, Porphyra tenera, Chondrus versicolor, Ephedra violaceus, Cytodon clitoris, Chondrus crispatus, Gelidium amansii, Gratelium brevicaulis, Gratelium bodies, Gracilaria platypodium, Gracilaria verrucosa, Gratelium brevifiliformis, Gracilaria platyphylla, Porphyra pteropilea (Gloiopeltis furcifera), Porphyra (Porphyra, Porphyra yezoensis), Gloiopeltis parviflora, Porphyra pendula, Porphyra spinosa, Porphyra hirta, Euglena, solieria robusta, Asiatic Grateloupia filicina, Gelidium amansii, Craicephalum purpureum, Gelidium amansii, etc. Among them, the sea tangle, the sea moss, the enteromorpha and the like are particularly preferable. Among these algae, some microalgae such as green algae have very strong cell walls, and thus it is sometimes difficult to form an insoluble dietary fiber microparticle complex described later. Therefore, it is preferable that the microalgae be used after pretreatment for breaking cell walls, or algae other than the microalgae be used.

The seed may be any seed as long as it contains insoluble dietary fiber in the edible part and/or the nonfood part. By way of example, mention may be made of: almonds, cashews, pecans (Pecan), macadamia nuts, pistachios, hazelnuts, coconut kernels, pine nuts, sunflower seeds, pumpkin seeds, watermelon seeds, castanea henryi, walnuts, japanese chestnuts, ginkgo biloba, sesame, brazil nuts, and the like, but are not limited thereto. Among them, preferred are almonds, cashews, macadamia nuts, pistachios, hazelnuts, coconut kernels, and the like.

The kind of beans is arbitrary as long as the beans contain insoluble dietary fibers in the edible part and/or the non-edible part. By way of example, mention may be made of: beans (Phaseolus vulgaris), kidney beans (Kidneybean), red beans, white beans, black beans, pinto beans, tiger beans, cotton beans (Limabean), string beans, peas (particularly unripe seeds, i.e., green peas), pigeon peas, mung beans, cowpeas, red beans, broad beans, soybeans (particularly young green beans), chickpeas, lentils (lentils), peanuts, lupins, tamarind beans, Carob beans (Carob), stinky beans, robinia beans, coffee beans, cacao beans, mexican bean and the like, but is not limited thereto. Among them, peas (particularly green peas which are unripe seeds), soybeans (particularly green beans), and the like are preferable. Although a processed product of cocoa beans, i.e., cocoa mass, can be used, the original flavor is hardly perceived because the husk and germ are removed in the production step and are fermented in the production step. Therefore, when cocoa beans are used, it is preferable to use cocoa beans having a form other than cocoa mass.

The cereal may be any cereal containing insoluble dietary fibers in the edible part and/or the non-edible part. By way of example, mention may be made of: corn (particularly preferably sweet corn), rice, wheat, barley, sorghum, oat, triticale, rye, buckwheat, Fonio (Fonio), quinoa, barnyard grass, millet, Giant corn (Giant corn), sugarcane, amaranth, and the like, but not limited thereto. Among them, corn (particularly, sweet corn), giant corn and the like are preferable.

The kind of the spices is arbitrary as long as it is spices containing insoluble dietary fibers in the edible part and/or the non-edible part. By way of example, mention may be made of: white pepper, red pepper, hot pepper (Capsicum frutescens), horseradish (horseradish), mustard, poppy seed, nutmeg, cinnamon, cardamom, cumin, crocus sativus, pimento, clove, Japanese pepper, orange peel, fennel, licorice, fenugreek, dill seed, zanthoxylum, capsicum annuum, olive fruit) and the like, but are not limited thereto. Among them, white pepper, red pepper, hot pepper and the like are particularly preferable.

As the food material containing insoluble dietary fiber, any food material including the various examples listed above can be appropriately selected and used, and particularly, it is preferably selected in consideration of the following characteristics.

As the food material containing insoluble dietary fiber, it is preferable to use a food material in which available carbohydrate is a predetermined value or more, from the viewpoint of formability of a microparticle complex described later in the composition. Specifically, the amount of available carbohydrate in the insoluble dietary fiber-containing food material is usually 2% or more, preferably 3% or more, more preferably 5% or more, particularly 7% or more, and particularly 10% or more. On the other hand, a food material such as sesame having a small monosaccharide amount (available carbohydrate is about 1% by mass) may be used, and from the viewpoint of formability of a microparticle complex described later in the composition, the available carbohydrate is preferably a food material having the above lower limit or more. In the case of using dried food as the insoluble dietary fiber-containing food as described below, the available carbohydrate after drying is preferably not less than the lower limit value. The amount of available carbohydrates in the food material is the total value of the components (starch, glucose, fructose, sucrose, maltose, lactose, galactose, trehalose) directly analyzed among the carbohydrates measured by the method described in the japanese food standard ingredient table, and the unit thereof can be "% (monosaccharide equivalent g/100 g)".

The water activity of the insoluble dietary fiber-containing food material is not particularly limited, but is preferably a predetermined value or less in view of the formability of a microparticle complex described later in the composition. Specifically, the water activity of the insoluble dietary fiber-containing food material is usually 0.95 or less, preferably 0.9 or less, more preferably 0.8 or less, and particularly preferably 0.65 or less. Since the water activity of ordinary fruits or vegetables tends to be higher than the above upper limit, when such food is used as the insoluble dietary fiber-containing food, it is preferable to use the food after drying treatment as described later. On the other hand, the lower limit of the water activity of the insoluble dietary fiber-containing food material is not particularly limited, but is usually 0.10 or more, preferably 0.20 or more, more preferably 0.30 or more, and particularly preferably 0.40 or more, from the viewpoint of easiness of storage and management. The water activity of the food material can be measured by a conventional method using a conventional water activity measuring apparatus.

The form of the food material containing insoluble dietary fiber is not particularly limited, and raw (fresh) food materials may be used, or food materials subjected to various treatments as described above (for example, drying, heating, alkali water removal, peeling, seed removal, ripening, salting, and pericarp processing) may be used. However, from the viewpoint of the formability of the particulate complex described later in the composition, it is preferable to use a food material subjected to a drying treatment in advance, that is, a dried food material. As the method for drying the food material, any method used for drying food materials can be generally used. By way of example, mention may be made of: solar drying, shade drying, freeze drying, air drying (e.g., hot air drying, fluidized bed drying, spray drying, drum drying, cryogenic drying, etc.), pressure drying, reduced pressure drying, microwave drying, oil heat drying, and the like. Among them, methods based on air drying (for example, hot air drying, fluidized bed drying, spray drying, drum drying, low-temperature drying, and the like) or freeze drying are preferable in terms of a small degree of change in color tone and flavor originally possessed by food materials and being capable of controlling flavor (scorched flavor and the like) other than food.

When the insoluble dietary fiber-containing food material is used in the composition of the present invention, the use ratio is not limited, and any ratio may be used depending on the type of food material or the content of the insoluble dietary fiber. However, it is preferable to use a composition containing the insoluble dietary fiber-containing food material at a ratio of not less than a certain ratio because the effect obtained by the application of the present invention is more remarkable. Specifically, the ratio of the total mass of the insoluble dietary fiber-containing food material in terms of dry mass to the total mass of the insoluble component (component insoluble in the composition) in terms of dry mass in the composition is usually 30% by mass or more, and among these, is preferably 50% by mass or more, more preferably 70% by mass or more, particularly 90% by mass or more, and particularly 100% by mass. When the composition is a food, the insoluble components contained therein are derived from food materials, and these food materials are classified into food materials containing insoluble dietary fibers and food materials other than the food materials (containing no insoluble dietary fibers), whereby the above ratio can be calculated. For example, in the case where a certain composition is a composition containing 20 parts by mass of fine particles of insoluble food fibers derived from a dried carrot as an insoluble food material, 30 parts by mass of dried tuna as a food material other than (containing no insoluble food fibers), and 50 parts by mass of water, the ratio of the insoluble food fiber-containing food material (carrot: 20 parts by mass) to the insoluble components (dried carrot + dried tuna: 50 parts by mass) is 40% by mass.

[ other food materials ]

The composition of the present invention may contain one or two or more kinds of optional food materials containing no insoluble dietary fiber, in addition to the above food materials containing insoluble dietary fiber. Examples of such food materials include: plant food materials, microbial food materials, animal food materials, and the like.

[ non-edible part and edible part of food materials ]

In the case where the food material used in the composition of the present invention, that is, the food material containing insoluble dietary fiber and/or the other (non-insoluble dietary fiber-containing) food material contains both an edible part and an inedible part, only the edible part may be used, only the inedible part may be used, or the edible part and the inedible part may be used together. In the present invention, the "inedible portion" of the food material means a portion of the food material that is unsuitable for normal diet or a portion that is discarded in accordance with normal dietary habits, and the "edible portion" means a portion obtained by removing a discarded portion (inedible portion) from the entire food material. In particular, in the case of a food material containing insoluble dietary fibers, a part containing insoluble dietary fibers is inferior in the ingestion property or blending property with other foods and is often discarded without being used for eating. In the present invention, the composition preferably contains the non-edible part in an amount of 0.1% by mass or more, more preferably 0.5% by mass or more, further preferably 0.8% by mass or more, further preferably 1.0% by mass or more, further preferably 2.0% by mass or more, and most preferably 3.0% by mass or more, on a wet weight basis. The upper limit of the above-mentioned mass ratio is usually 98 mass% or less, and among them, 91 mass% or less, further 85 mass% or less, particularly 80 mass% or less, and particularly 55 mass% or less.

The edible part and/or the non-edible part of the insoluble dietary fiber-containing material used in the composition of the present invention may be derived from a single kind of insoluble dietary fiber-containing material, respectively, or may be any combination of materials derived from a plurality of insoluble dietary fiber-containing materials. Further, when the edible part and the inedible part are contained together, the taste quality of the edible part is improved by setting the ratio of "inedible part/(edible part + inedible part)" to 0.2% or more, and therefore, it is preferably 0.5% or more, more preferably 0.8% or more, more preferably 1.0% or more, more preferably 2.0% or more, and most preferably 3.0% or more. The upper limit of the above proportion is usually 100% or less, and among them, 90% or less, further 80% or less, particularly 70% or less, and particularly 60% or less is preferable.

In addition, in the case where the composition of the present invention contains both the edible part and the non-edible part of the insoluble dietary fiber-containing material, these edible part and non-edible part may be derived from different kinds of insoluble dietary fiber-containing materials, respectively, but preferably contains the edible part and the non-edible part derived from the same kind of insoluble dietary fiber-containing material. That is, by using a part or all of the edible part and a part or all of the inedible part derived from the same kind of food material containing insoluble dietary fiber, the nutrition of such food material containing insoluble dietary fiber can be ingested without waste. In particular, the composition of the present invention can improve astringency attributable to insoluble dietary fibers as described later, and therefore, such an inedible portion of a food material containing a large amount of insoluble dietary fibers can be easily ingested without waste.

Examples of the inedible part of the food material containing insoluble dietary fiber include the skin, seed, core, lees and the like of the above-mentioned various food materials containing insoluble dietary fiber. Among them, corn (e.g., sweet corn), hot pepper, pumpkin, beet, broccoli, green bean (branch bean), tomato, rice, onion, cabbage, apple, grape, sugarcane, citrus (e.g., satsuma mandarin, orange, etc.), etc., can be suitably used in the present invention because of abundant residual nutrients, but not limited thereto. Specific examples of the non-edible part of the food material containing insoluble dietary fiber include: the husk, pistil and cob (core) of corn (e.g., sweet corn, etc.), seed and pedicle of capsicum, seed or flesh of pumpkin, skin of beet, stem and leaf of broccoli, pod (hull) of green bean (branch bean), pedicle of tomato, rice hull of rice (rice), skin (protective leaf) of onion, pan and head, core of cabbage, core of apple, pericarp and seed of grape, bagasse of sugarcane, skin, seed and tangerine of citrus (e.g., wenzhou mandarin orange, fragrant orange, etc.), but not limited thereto. Further, it is preferable that the composition does not contain components harmful to the human body to such an extent that they affect the human body.

In the case where the composition of the present invention contains other (non-insoluble dietary fiber) food materials in addition to the food materials containing insoluble dietary fiber, the edible part and/or the non-edible part thereof may be optionally used in combination as in the case of the food materials containing insoluble dietary fiber.

It is needless to say that the part or ratio of the non-edible part in the food material used in the composition of the present invention, that is, the food material containing insoluble dietary fiber and/or the other food material (containing no insoluble dietary fiber) is a part or ratio that can be understood by those skilled in the art as long as the food or processed food is treated. For example, the "waste portion" and the "waste ratio" described in the japanese food standard ingredients table 2015 year edition (seventh edition) may be referred to, and these portions and ratios may be regarded as the portions and ratios of the inedible portions. Table 1 below lists examples of food materials containing insoluble dietary fibers and "waste parts" and "waste ratios" (i.e., parts and ratios of inedible parts) of these food materials described in the japanese food standard ingredients table 2015 year edition (seventh edition). The position or ratio of the edible portion can be understood from the position or ratio of the non-edible portion in the food material.

[ Table 1]

[ oil and fat ]

The composition of the present invention may contain one or two or more kinds of oils and fats. The type of the oil or fat may be one or two or more of various fatty acids (e.g., linoleic acid, linolenic acid, oleic acid, palmitic acid, stearic acid, caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, pentadecanoic acid, etc.) and is preferably an edible oil or fat, a food material containing an edible oil or fat, a food material using an edible oil or fat as a raw material, or the like.

Examples of the edible oil and fat include: sesame oil, rapeseed oil, high oleic rapeseed oil, soybean oil, Palm stearin, Palm olein, Palm kernel oil, Palm fractionated oil (PMF), cottonseed oil, corn oil, sunflower oil, high oleic sunflower oil, safflower oil, olive oil, linseed oil, rice bran oil, camellia oil, perilla oil, flavor oil, coconut oil, grape seed oil, peanut oil, almond oil, avocado oil, salad oil, rapeseed oil, fish oil, beef tallow, lard, chicken oil, or MCT (Medium Chain Triglyceride), diglycerides, hydrogenated oils, interesterified oils, milk fat, Ghee (Ghee), cocoa butter, and the like. Among them, liquid edible oils and fats such as sesame oil, olive oil, rapeseed oil, soybean oil, milk fat, sunflower seed oil, rice bran oil, palm olein and the like are preferable because they have an effect of improving the smoothness of the composition. On the other hand, fats and oils other than cacao butter are preferably used from the viewpoint of workability in production. One kind of these edible oils and fats may be used, or two or more kinds thereof may be used in combination. The edible oil or fat is preferably an edible oil or fat in which the ratio of unsaturated fatty acids (the total ratio of monounsaturated fatty acids and polyunsaturated fatty acids) is greater than the ratio of saturated fatty acids, and therefore, the refining treatment can be effectively performed, and therefore, it is more preferable that the ratio of unsaturated fatty acids is greater than 2 times the ratio of saturated fatty acids.

On the other hand, examples of the food material using an edible oil or fat as a raw material include: butter, margarine, shortening, whipped cream, and soymilk cream (for example, "kokulimu" (registered trademark) of shinko corporation), etc.). The food material which is liquid at room temperature is preferable in terms of convenience. In addition, among the above-mentioned food materials containing insoluble dietary fibers and other food materials, food materials containing edible oil and fat may be used for such a purpose. One of these food materials may be used, or two or more of these food materials may be used in combination.

However, from the viewpoint of improving the compatibility of the food material, it is preferable to separately add the extracted and purified edible oil or fat to the food material regardless of whether the oil or fat is contained in the food material containing insoluble dietary fiber or other food materials. Specifically, it is preferable that the total content of the oil and fat components contained in the composition of the present invention is usually 10% by mass or more, and 30% by mass or more of the total content is derived from an edible oil and fat subjected to extraction and purification treatment.

In the composition of the present invention, the total oil content is preferably a certain value or less, from the viewpoint of forming a particulate composite described later in the composition as appropriate. Here, the total fat component content of the composition means the content of a fat component derived from the total components including the total food materials contained in the composition. Specifically, the upper limit of the total oil component content of the composition of the present invention is usually less than 20% by mass, preferably less than 15.5% by mass, and more preferably less than 10.5% by mass. On the other hand, the lower limit of the total oil component content of the composition of the present invention is not limited, but is usually 0.1 mass% or more, more preferably 0.2 mass% or more, and particularly preferably 0.3 mass% or more, in view of rapidly forming a particulate composite described later in the composition.

[ seasoning/food additive, etc. ]

The composition of the present invention may contain any one or two or more kinds of seasonings/food additives and the like. Examples of the seasoning/food additive and the like include: soy sauce, miso, alcohols, saccharides (e.g., glucose, sucrose, fructose, glucose fructose, fructose glucose syrup, etc.), sugar alcohols (e.g., xylitol, erythritol, maltitol, etc.), artificial sweeteners (e.g., sucralose, aspartame, saccharin, acesulfame potassium, etc.), minerals (e.g., calcium, potassium, sodium, iron, zinc, magnesium, etc., and salts thereof, etc.), flavors, pH adjusters (e.g., sodium hydroxide, potassium hydroxide, lactic acid, citric acid, tartaric acid, malic acid, acetic acid, etc.), cyclodextrins, antioxidants (e.g., vitamin E, vitamin C, tea extract, green coffee bean extract, chlorogenic acid, spice extract, caffeic acid, rosemary extract, vitamin C palmitate, rutin, quercetin, bayberry extract, sesame extract, etc.), emulsifiers (as examples, glycerin fatty acid ester, acetic acid monoglyceride, lactic acid monoglyceride, citric acid monoglyceride, diacetyl tartaric acid monoglyceride, succinic acid monoglyceride, polyglycerol fatty acid ester, polyglycerol polyricinoleate, quillaia saponaria extract, soyasaponin, tea seed saponin, sucrose fatty acid ester, etc.), colorant, thickening stabilizer, etc.

However, due to recent enhancement of natural consciousness, the composition of the present invention preferably does not contain a so-called emulsifier and/or colorant and/or thickening stabilizer (for example, substances described as "colorant", "thickening stabilizer" and "emulsifier" in "food additive name table for display" of food additive display sleeve book (2011 edition)). Among them, the composition of the present invention preferably contains no emulsifier from the viewpoint of quality of making the taste of the raw material easily perceived. In particular, it is desirable that the composition of the present invention does not contain a food additive (for example, a substance used for food additive applications described in "food additive substance name table for display" in the food additive display book (2011 edition)). In addition, it is preferable not to add a saccharide (glucose, sucrose, fructose, glucose fructose, fructose-fructose liquid sugar, fructose-glucose liquid sugar, or the like) from the viewpoint of being easily susceptible to the sweetness of the food itself. Moreover, the composition of the present invention may be a solution not containing acetic acid in order to easily feel the taste of the raw material.

[ Water ] A

Moisture is preferably included in the composition of the present invention. The water in the composition may be water derived from the above-mentioned components of the composition, or may be further added in the form of water. In the present invention, the moisture content of the composition means the total amount of moisture derived from the various components of the composition and the amount of moisture to be added separately.

Specifically, the mass ratio of the moisture content to the entire composition is usually 35% by mass or more, preferably 45% by mass or more, more preferably 50% by mass or more, and particularly 55% by mass or more. When the mass ratio of the water content to the entire composition is not less than the lower limit, the shape of the microparticle composite can be easily controlled, which is preferable. On the other hand, the upper limit of the mass ratio of the moisture content is not limited, but it is usually 98 mass% or less, further 96 mass% or less, and of these, 90 mass% or less, which is convenient from the viewpoint of industrial productivity.

In the composition of the present invention, the ratio of the moisture content to the total of the moisture content and the total oil content, that is, the value of "moisture content/(moisture content + total oil content)" is usually 75% or more, more preferably 80% or more, and particularly preferably 85% or more, from the viewpoint of suitably forming a particulate composite described later in the composition. On the other hand, the upper limit of the value of "moisture content/(moisture content + total oil and fat component content)" is not limited, but is preferably 100 mass% or less in view of rapid formation of a fine particle composite described later in the composition.

[ microparticles and microparticle composites ]

In the composition of the present invention, the insoluble dietary fiber is present in the form of microparticles. The microparticles may be formed of only one or two or more insoluble dietary fibers, or may be formed of one or two or more insoluble dietary fibers and one or two or more other components.

Further, in the composition of the present invention, a plurality of the above-mentioned microparticles comprising insoluble dietary fiber are aggregated to form a complex which can be broken by agitation. That is, the composition of the present invention contains a microparticle complex comprising insoluble dietary fibers. The composition of the present invention contains insoluble dietary fibers in such a state as a complex, and therefore, the composition is suppressed in moisture separation, improved in texture, easy to ingest, and excellent in compatibility with other foods. In the present invention, unless otherwise specified, ultrasonic treatment is assumed as a typical example of disturbance from the outside to break up the microparticle composite. In the present invention, "ultrasonic treatment" means a treatment of applying ultrasonic waves having a frequency of 40kHz for 3 minutes to a measurement sample at an output of 40W unless otherwise specified.

The composition of the present invention can provide a composition having various advantageous characteristics such as improvement in stability of the composition (prevention of drying) and improvement in emulsifying capacity by adjusting the form, size, and the like of the particulate complex before and after application of a disturbance to a range described below while containing the particulate complex containing insoluble dietary fibers. The reason is not clear, but is considered as follows: the composite is formed into a characteristic shape as if a plurality of dietary fibers are interlaced in the composition, and the composite exerts various effects. Recently, research on micronization techniques has been actively conducted in various fields including the field of food, but characteristics obtained by the shape of a secondary structure (composite) formed by aggregating micronized microparticles have not been known so far. It is not to be said that the various effects which have been heretofore unknown are exhibited by adjusting the form, size, and the like of such a microparticle complex, and it has been hitherto unknown at all.

[ particle diameter in composition ]

The composition of the present invention preferably satisfies the following specific requirements with respect to the particle size of the particulate composite and the particles contained in the composition before and after the perturbation, i.e., the maximum particle size, the mode particle size, and d50 for the particle size. That is, the composition of the present invention contains a plurality of microparticle complexes in a state where no disturbance is applied, that is, in a state before ultrasonic treatment, whereas in a state where disturbance is applied, that is, in a state after ultrasonic treatment, a part or all of the microparticle complexes are disintegrated to form individual microparticles, not only the maximum particle diameter is largely changed before ultrasonic treatment but also various parameters related to the particle diameter such as the mode particle diameter and d50 of the particle diameter are largely changed.

The maximum particle size of the particulate composite before the disturbance in the composition of the present invention is adjusted to be within a prescribed range. Specifically, the maximum particle diameter of the composition of the present invention before the perturbation, that is, before the ultrasonic treatment is usually 100 μm or more. Among them, it is preferably 110 μm or more. By setting the maximum particle size of the composition before ultrasonic treatment to the lower limit or more, it is possible to prevent the texture of the food material from being destroyed and impart an undesirable flavor. On the other hand, the maximum particle size of the composition of the present invention before the perturbation, that is, before the ultrasonic treatment is not limited, is usually 2000 μm or less, and among them, 500 μm or less is preferable. It is convenient for the reason of industrial productivity to set the maximum particle diameter of the composition before the ultrasonic treatment to the upper limit or less.

The maximum particle size of the perturbed microparticle complex in the composition of the present invention is adjusted to be within a specific range. Specifically, the maximum particle diameter of the composition of the present invention after the perturbation, that is, after the ultrasonic treatment is usually 20 μm or more, and preferably 30 μm or more. When the maximum particle size of the composition after the ultrasonic treatment is not less than the lower limit, it is preferable for the reason that the texture of the food material is not easily destroyed and an undesirable flavor is imparted. On the other hand, the maximum particle size of the composition of the present invention after the perturbation, that is, after the ultrasonic treatment is not limited, and is usually 1100 μm or less, and preferably 800 μm or less. It is convenient for the reason of industrial productivity to set the maximum particle diameter of the composition after the ultrasonic treatment to the upper limit or less.

Since the composition of the present invention is a suspension system, it is difficult to accurately determine the maximum particle size by visual observation, but at least the lower limit of the maximum particle size can be roughly determined by visual observation. That is, it is considered that when the maximum particle diameter observed with a microscope is larger than a certain value, there is a high possibility that the actual maximum particle diameter is also larger than the certain value.

The mode particle diameter (mode diameter) of the particulate composite before the disturbance in the composition of the present invention is adjusted to be within a predetermined range. Specifically, the mode particle size of the composition of the present invention before the disturbance, that is, before the ultrasonic treatment is usually 5 μm or more. Among them, it is preferably 10 μm or more, and more preferably 12 μm or more. When the mode particle size of the composition before ultrasonic treatment is not less than the above lower limit, the composition has a quality that is not easily separated from water, and is preferable from the viewpoint of commercial distribution. On the other hand, the mode particle size of the composition of the present invention before the disturbance, that is, before the ultrasonic treatment is usually 400 μm or less. Among them, it is preferably 300 μm or less, more preferably 200 μm or less, particularly preferably 100 μm or less. By setting the mode particle size of the composition before ultrasonic treatment to the upper limit or less, deterioration in texture can be prevented, and appropriate texture and feeling upon eating can be imparted to the composition.

The mode particle diameter of the particulate composite after the disturbance in the composition of the present invention is also adjusted to be within a predetermined range. Specifically, the mode particle diameter of the composition of the present invention after the disturbance, that is, after the ultrasonic treatment is usually 0.3 μm or more. Among them, it is preferably 1.0 μm or more, more preferably 3.0 μm or more, particularly preferably 5.0 μm or more, particularly preferably 7.0 μm or more. When the mode particle diameter of the composition after the ultrasonic treatment is not less than the above lower limit, the composition has a quality of being not easily dried and can be stored for a long period of time, which is preferable. On the other hand, the mode particle diameter of the composition of the present invention after the disturbance, i.e., after the ultrasonic treatment is usually 100 μm or less. Among them, it is preferably 90 μm or less, further 80 μm or less, particularly 70 μm or less, or 60 μm or less, particularly 50.0 μm or less. When the mode particle size of the composition after ultrasonic treatment is not more than the upper limit, deterioration in texture can be prevented, and appropriate texture and feeling upon eating can be imparted to the composition.

In the present invention, the mode particle diameter means a particle diameter of a channel in which the particle frequency% is the largest in the particle diameter distribution of each channel obtained by measuring the composition using a laser diffraction particle size distribution measuring apparatus. In the case where there are a plurality of channels of the same exact particle frequency%, the particle diameter of the channel in which the particle diameter is smallest is employed. If the particle size distribution is a normal distribution, the value is the same as the median diameter, but if there is unevenness in the particle size distribution, particularly if there are a plurality of peaks in the particle size distribution, the numerical value is greatly different. The measurement of the particle size distribution of the sample by the laser diffraction particle size distribution measuring apparatus can be carried out, for example, by the following method. In the case where the sample is a thermoplastic solid, the sample is heated to be in a liquid state and then subjected to analysis, and this can be subjected to analysis by a laser analysis type particle size distribution measuring apparatus.

In addition to the maximum particle diameter and the mode particle diameter described above, d50 (50% cumulative diameter, median diameter) of the particle diameter of the particulate composite before and after the disturbance in the composition of the present invention is preferably adjusted to fall within a predetermined range. Specifically, the d50 of the particle size of the composition of the present invention before the perturbation, i.e., before the ultrasonic treatment, is usually 5 μm or more, preferably 10 μm or more, and usually 400 μm or less, preferably 300 μm or less, more preferably 250 μm or less, and particularly 200 μm or less. The d50 of the particle size after the disturbance, i.e., after the ultrasonic treatment, of the composition of the present invention is usually not less than 1 μm, preferably not less than 5 μm, more preferably not less than 7 μm, and usually not more than 150 μm, more preferably not more than 100 μm, more preferably not more than 75 μm. The particle size d50 of the composition is defined as follows: when the particle size distribution of the composition is divided into two parts according to a certain particle size, the ratio of the cumulative value of the greater-side particle frequency% to the cumulative value of the smaller-side particle frequency% is 50: 50 particle size. The d50 of the particle size of the composition can be measured, for example, using a laser diffraction particle size distribution measuring apparatus described later.

Unless otherwise specified, "particle size" in the present invention means a particle size measured on a volume basis. In addition, "particles" in the present invention means a concept including not only individual fine particles but also a fine particle composite in which they are aggregated, unless otherwise specified.

The measurement conditions for various parameters related to the particle size of the present invention are not limited, and the following conditions may be used. First, any solvent can be used as the solvent for measurement as long as it is a solvent that hardly affects the structure of insoluble dietary fibers in the composition. By way of example, distilled water is preferably used. The laser diffraction particle size distribution measuring apparatus used for the measurement is not limited, and for example, a Microtrac MT3300 EXII system available from Microtrac bel corporation can be used. The measurement application software is not limited, and for example, DMS2(Data Management System version2, MicrotracBEL co., ltd.) can be used. In the case of using the above-described measurement device and software, during measurement, the washing button of the software is pressed to perform washing, then the Setzero button of the software is pressed to perform zero adjustment, and the sample is directly put in until the concentration of the sample reaches an appropriate range by sample loading. The sample before the disturbance, that is, the sample which was not subjected to the ultrasonic treatment, was adjusted to a concentration within an appropriate range within 2 sample loads after the sample was put in, and immediately thereafter, laser diffraction was performed at a flow rate of 60% for a measurement time of 10 seconds, and the obtained result was used as a measurement value. On the other hand, when a disturbed sample, that is, a sample subjected to ultrasonic treatment is measured, a sample subjected to ultrasonic treatment in advance may be put in, or after the sample is put in, ultrasonic treatment may be performed using the above-described measuring apparatus, and then the measurement may be performed. In the latter case, a sample that has not been subjected to ultrasonic treatment is put in, the concentration is adjusted to an appropriate range by sample loading, and then ultrasonic treatment is performed by pressing an ultrasonic treatment button of the software. After that, after 3 times of defoaming treatment, sample loading treatment was performed again, and it was confirmed that the concentration was still in an appropriate range, laser diffraction was rapidly performed at a flow rate of 60% for a measurement time of 10 seconds, and the obtained result was used as a measurement value. As parameters for measurement, for example, the following can be set: and (3) distribution display: volume, particle refractive index: 1.60, solvent refractive index: 1.333, 2000.00 μm as an upper limit of measurement (μm), and 0.021 μm as a lower limit of measurement (μm).

Specifically, the particle frequency of each channel (hereinafter referred to as "particle frequency% of ○○ channel") can be obtained by measuring the particle frequency of all channels in the measurement range as denominator, and the particle frequency% of each channel (hereinafter referred to as "particle frequency% of ○○ channel") can be obtained by measuring the particle frequency of each channel (hereinafter referred to as "frequency% of particles") individually for each channel in table 2, as the particle frequency% of 1 channel, for example, indicates the frequency% of particles of 2000.00 μm or less and larger than 1826.00 μm, and particularly, with respect to the maximum particle diameter, the particle frequency% of each of 132 channels in table 2 can be measured, and the obtained result is the particle diameter of the channel having the largest particle diameter among the channels for which the particle frequency% is confirmed, and in other words, the particle diameter of the composition of the present invention is measured as the maximum particle diameter of 2000.00, and the sample is measured as the maximum particle diameter of the sample after the sample is put into the distillation apparatus.

[ specific surface area of particles in composition ]

The composition of the present invention preferably satisfies the above-described various requirements, and the specific surface area per unit volume of the particles (microparticles and microparticle composites) in the composition before and after the application of the disturbance, that is, before and after the ultrasonic treatment satisfies the following requirements. That is, the composition of the present invention contains a plurality of microparticle complexes in a state in which no disturbance is applied, that is, in a state before the ultrasonic treatment, whereas in a state in which disturbance is applied, that is, in a state after the ultrasonic treatment, a part or all of the microparticle complexes are disintegrated to be individual microparticles, the specific surface area per unit volume is also greatly changed between before the ultrasonic treatment and after the ultrasonic treatment.

I.e. the specific surface area per unit volume (gamma) of the particles (microparticles and microparticle composites) in the composition before the application of the perturbation, i.e. before the ultrasonic treatment_B) Typically 1.00m²A volume of 0.80m or less, preferably²Is less than/mL. If the specific surface area (. gamma.) is set_B) When the content is not more than the upper limit, the fine particles form a composite sufficiently, and the stability-improving effect of the present invention is sufficiently exhibited, which is preferable. The specific surface area (. gamma.) is_B) The lower limit of (B) is not particularly limited, but is usually 0.07m in view of enhancing the effect of improving the stability of the composition²A volume of 0.10m or more, preferably²A volume of 0.15m or more per mL²A value in a range of not less than mL.

In addition, the specific surface area per unit volume (γ) of the particles (microparticles and microparticle composites) in the composition after the application of the perturbation, i.e., after the ultrasonic treatment_A) Typically 1.70m²A volume of 1.50m or less, preferably²A volume of 1.30m or less per mL²A volume of 1.10m or less per mL²Less than/mL, wherein the particle size is 0.80m²Is less than/mL. If the specific surface area (. gamma.) is set_A) When the content is not more than the upper limit, the fine particles form a composite sufficiently, and the stability-improving effect of the present invention is sufficiently exhibited, which is preferable. Further, the specific surface area (. gamma.) is adjusted to_A) The lower limit of (B) is not particularly limited, but is usually 0.07m in view of enhancing the effect of improving the stability of the composition²A volume of 0.10m or more, among them²A volume of 0.15m or more per mL²More than mL, wherein the particle size is 0.20m²A value in a range of not less than mL.

In addition, the ratio of the specific surface area per unit volume of the particles (microparticles and microparticle composites) in the composition before and after the application of the disturbance, that is, before and after the ultrasonic treatment, that is, (γ)_B/γ_A) Satisfying the specified range. Specifically, (γ)_B/γ_A) Usually, 0.80 or less is preferable. By making gamma_B/γ_AThe content of the above-mentioned upper limit or less is preferably because the dietary fibers form a composite well with each other and the effect of improving the stability of the composition is appropriately exhibited. In addition, the pair (gamma)_B/γ_A) The lower limit of (b) is not particularly limited, but is usually preferably 0.1 or more.

In the present invention, the specific surface area per unit volume of the composition means a specific surface area per unit volume (1mL) when the particles are assumed to be spherical, which is measured by a laser diffraction particle size distribution measuring apparatus. The specific surface area per unit volume when the particles are spherical is a value based on a measurement mechanism different from a measurement value (specific surface area per volume and per mass obtained by a permeation method, a gas adsorption method, or the like) reflecting the components, the surface structure, or the like of the particles. The specific surface area per unit volume when the particles are spherical can be obtained by 6 × Σ (ai) ÷ Σ (ai · di) assuming that the surface area per 1 particle is ai and the particle diameter is di.

[ morphological characteristics in the composition ]

The composition of the present invention satisfies all of the following requirements (1) to (3) that specify the form of microparticles and microparticle composites containing insoluble dietary fibers contained therein, including at least 1 or more, preferably 2 or more, and more preferably 3.

< requirement (1): the value N (I) >

The requirement (1) is to set a numerical value n (I) obtained by the following formula (I) to a predetermined value or more.

(math formula 1)

N(I)＝(α/β) (I)

Wherein, in the formula (I),

β represents a 90% numerical value of the "minor axis" before ultrasonic treatment measured by the particle shape image analyzer.

In other words, the composition containing the particulate composite satisfying the requirement (1), i.e., the numerical value n (i) of the predetermined value or more, means a composition having predominantly fine particles having morphology characteristics that the major axis is longer (elongated) than the minor axis, and the proportion thereof is higher than that of a usual composition.

Specifically, the numerical value n (i) is usually 1.20 or more, preferably 1.30 or more, more preferably 1.40 or more, particularly 1.50 or more, depending on the requirement (1). When the value n (i) is not less than the lower limit, the effect of improving the emulsifying capacity of the composition and improving the astringency can be obtained, and therefore, it is preferable.

The upper limit of the logarithmic value n (i) is not limited, but is usually 4.0 or less, preferably 3.0 or less, from the viewpoint of convenience in production.

Further, since the effect of improving the astringency of the composition can be confirmed by performing the micronization treatment until the value n (i) is increased by 5% or more before and after the micronization, the micronization treatment is preferably further performed until the increase is 10% or more, preferably 15% or more, and most preferably 20% or more. That is, the effect of improving astringency or the like can be remarkably confirmed with respect to the composition in a state in which the micronization treatment is performed until the value n (i) is increased by 5% or more before and after micronization. For example, when the value n (i) of the composition before the media-agitating mill treatment (corresponding to test examples 10, 15, 25, and the like described later) is, for example, 1.24 (test example 10) and the value n (i) of the composition after the corresponding micronization treatment by the media-agitating mill (corresponding to test examples 11 to 13, 16 to 18, 26 to 28, and the like described later) is, for example, 1.54 (test example 11), the micronization treatment may be performed until the value n (i) increases by about 24%.

< requirement (2): the value N (II) >

The requirement (2) is to set the numerical value n (II) obtained by the following formula (II) to a predetermined value or more.

(math figure 2)

N(II)＝(α/β)/ω (II)

Wherein, in the formula (II),

ω represents a 10 percentile numerical value of "unevenness" before ultrasonic treatment measured by the particle shape image analysis device.

In other words, the composition containing the fine particle composite satisfying the requirement (2), that is, the numerical value n (ii) of the predetermined value or more, means a composition having predominantly fine particles having morphology characteristics that the major axis is long (slender) with respect to the minor axis and the surface of the particles is uneven, and the ratio thereof is higher than that of a normal composition.

Specifically, the numerical value n (ii) is usually 1.40 or more, and among them, preferably 1.50 or more, particularly 1.60 or more, further 1.70 or more, or 1.80 or more, or 1.90 or more, particularly 2.00 or more, according to the requirement (2). When the value n (ii) is not less than the lower limit, the effect of improving the emulsifying capacity of the composition and improving the astringency can be obtained, and therefore, it is preferable.

The upper limit of the logarithmic value n (ii) is not limited, but is usually 4.0 or less, preferably 3.0 or less, from the viewpoint of convenience in production.

Further, since the effect of improving the astringency of the composition can be confirmed by performing the micronization treatment until the value n (ii) is increased by 5% or more before and after the micronization, the micronization treatment is preferably further performed until the increase is 10% or more, more preferably 20% or more, and most preferably 30% or more. That is, the effect of improving astringency or the like can be remarkably confirmed with respect to the composition in which the micronization treatment is performed until the value n (ii) is increased by 5% or more before and after micronization. For example, when the value n (ii) of the composition before the media-agitating mill treatment (corresponding to test examples 10, 15, 25, etc., which will be described later) is, for example, 1.43 (test example 10) and the value n (ii) of the composition after the corresponding micronization treatment by the media-agitating mill (corresponding to test examples 11 to 13, 16 to 18, 26 to 28, etc., which will be described later) is, for example, 2.34 (test example 11), the micronization treatment can be performed until the value n (ii) increases by about 63%.

< requirement (3): the value N (III) >

The requirement (3) is to set the numerical value n (III) obtained by the following formula (III) to a predetermined value or more.

(math figure 3)

N(III)＝(α/β)×γ_A(III)

Wherein, in the above formula (III),

In other words, the composition containing fine particles that satisfies the requirement (3), i.e., the numerical value n (iii) is a composition having a higher proportion than that of a normal composition, and mainly including fine particles having a morphology characterized by a longer (elongated) major axis relative to a minor axis and a larger specific surface area per unit volume after aggregation and disintegration by ultrasonic treatment.

Specifically, the numerical value n (iii) is usually 0.50 or more, preferably 0.60 or more, particularly 0.70 or more, further 0.80 or more, or 0.90 or more, particularly 1.00 or more, depending on the requirement (3). When the value n (iii) is not less than the lower limit, the effect of improving the emulsifying capacity of the composition and improving the astringency can be obtained, and therefore, it is preferable.

The upper limit of the logarithmic value n (iii) is not limited, but is usually 4.0 or less, preferably 3.0 or less, from the viewpoint of convenience in production.

Further, since the effect of improving the astringency of the composition can be confirmed by performing the micronization treatment until the value n (iii) is increased by 5% or more before and after the micronization, the micronization treatment is preferably further performed until the increase is 10% or more, more preferably still 20% or more, further preferably 30% or more, and most preferably 40% or more. That is, the effect of improving astringency or the like can be remarkably confirmed with respect to the composition in a state in which the micronization treatment is performed until the value n (iii) is increased by 5% or more before and after micronization. For example, when the value n (iii) of the composition before the media-agitating mill treatment (corresponding to test examples 10, 15, 25, etc., which will be described later) is, for example, 0.54 (test example 10) and the value n (iii) of the composition after the corresponding micronization treatment by the media-agitating mill (corresponding to test examples 11 to 13, 16 to 18, 26 to 28, etc., which will be described later) is, for example, 1.31 (test example 11), the micronization treatment may be performed until the value n (iii) increases by about 142%.

< method for measuring morphological requirements >

In the present invention, the measurement of the long diameter, short diameter and unevenness of the particles (fine particles and fine particle composite) in the composition, which are various parameters for calculating n (i) to n (iii) described above, can be performed by planar image analysis using a particle shape analyzer. For example, in order to grasp the accurate morphological characteristics of the fine particle image, the following method is preferably employed. That is, it is preferable to use a particle shape analyzer having a function of capturing an image of a normal single particle and analyzing the shape thereof, for example, to flow a composition as a powder/granular suspension in a flow tank, automatically discriminate a fine particle complex entering the field of capture, grasp the morphological characteristics thereof, and analyze the complex. Here, it is preferable to use a particle shape analysis apparatus capable of randomly extracting a microparticle composite and automatically obtaining a large amount of single particle information in a short time. Specifically, a particle analyzer (for example, PITA-4 manufactured by Seishin corporation, ltd.) which is a particle analysis type apparatus based on a moving image analysis method and can be provided with a high-pixel camera is preferably used.

Specifically, the particles (microparticles and microparticle complexes) in the composition can be captured using a camera capable of capturing detailed images of the particles. Among them, an imaging camera (CCD (Charge Coupled Device) camera or a C-MOS (Complementary Metal Oxide Semiconductor) camera) capable of capturing a planar image having a specific effective pixel number of 1920(H) × 1080(V) and a pixel size of about 2.8 μm × 2.8 μm in detail is preferably used. An example of such an Imaging camera is DMK33UX290 (manufactured by The Imaging Source company). As the conditions for image capturing, for example, the following conditions can be adopted. That is, as an objective lens for image capturing, an objective lens of 4-fold magnification was used, and an image of the microparticle particle was captured while the sample was caused to flow at an appropriate flow rate. In particular, the shape of the flow channel can be accurately grasped by using a planar expansion groove which can improve the planar expansion effect and allow most of the center of the compound in the composition before ultrasonic treatment to pass through the focal range of the lens. In taking an image, the conditions of the particle image analysis apparatus are set to the following degrees: the focus is set appropriately so that the particle shape can be clearly confirmed and the contrast with the background is set to such an extent that the complex in the composition before ultrasonic treatment can be clearly distinguished from the background. As an example of setting various parameters when acquiring an image, when an imaging camera of 8-Bit gray scale (0 is black and 255 is white) is used, a planar image can be acquired with an LED intensity of 100 and a camera gain of 100db, and then the brightness level of a particle image existing therein is set to 115 and the contour level of the image is set to 160. As the solvent or carrier liquid for measurement, any solvent may be used as long as it does not affect the form of the particulate composite in the composition, and distilled water is preferable as an example. For example, the sample may be diluted 1000 times with a solvent used for measurement, and injected into a cell for particle image measurement (synthetic quartz glass) to be subjected to the microparticle complex shape image analysis. Image capturing is performed as a planar image (pixel size 2.8 μm × 2.8 μm) of 1920 pixels × 1080 pixels, for example, and can be performed until the number of particles to be captured reaches 10000 samples, for example. It should be noted that if the focus of the captured image is not appropriately adjusted, the shape of the captured image cannot be accurately measured, and therefore, the image is captured with the focus of the captured image sufficiently aligned. Further, since the setting of the imaging conditions varies depending on the imaging, it is desirable to readjust to appropriate conditions for each imaging and then perform imaging again.

The image analysis of the particles (microparticles and microparticle complexes) in the composition to be captured can be performed, for example, in the following order. That is, for a fine particle image having a minimum number of pixels of 15 or more existing in a plane image, a major axis, a minor axis, and an irregularity were measured for 10000 images, respectively, and the major axis and the minor axis were 90% of 10000 samples, and the irregularity was 10% of 10000 samples. In the present invention, the "percentile value" refers to a value obtained by arranging the distribution of measured values from a smaller number to a larger number and locating the distribution at an arbitrary% from the smaller number. For example, a value of 90% of arbitrarily measured values in the case of measuring 10000 fine particle images means a value measured at 9000 th from the smaller value among the measured values in all the fine particle images.

In the present invention, the "major axis" and the "minor axis" of the particles (microparticles and microparticle composites) in the composition may be determined by a particle shape formed by connecting pixels adjacent to each other in the longitudinal and lateral directions of the particle image, that is, the "major axis" of the particles indicates the maximum distance between 2 points on the contour line in the particle shape on the particle image, and the "minor axis" of the particles indicates the shortest distance in the case where the particle shape is sandwiched by 2 straight lines parallel to the straight line along the maximum distance in the particle shape of the particle image, that is, the more the microparticles or microparticle composites having a strong specific morphological feature such as a slender morphological feature are, the more the tendency is reflected in each 90 percentile value representing the dominant feature of the major axis and the minor axis of the composition, and n (i) (i.e., the 90 percentile value of the major axis (α)/the 90 percentile value of the minor axis (β)) becomes larger.

In the present invention, the "degree of concavity and convexity" of the particles (fine particles and fine particle composites) in the composition is a value indicating the degree of concavity and convexity of the particle shape on the particle image, and is obtained by dividing (the perimeter length when the apexes of the convex portions of the particle shape on the particle image are connected by the shortest distance) ÷ (the contour length of the particle shape on the particle image) —, that is, the more particles having a specific morphological feature such that there are many concavities and convexities on the particle surface, the more this tendency is reflected in the 10 percentile value of the degree of concavity and convexity reflecting the overall feature of the composition in a state in which a disturbance is applied, that is, the more particles having a slender morphological feature and having concavities and convexities on the particle surface, the greater this tendency is reflected in the 90 percentile value reflecting the dominant features of the long diameter and short diameter of the composition, and the 10 percentile value of the degree of concavity and convexity (ω), and as a result, the value n (ii) (that is, the 90 percentile value of the long diameter (α)/the short diameter (β)) becomes larger.

[ content of particulate composite ]

In the composition of the present invention, the content of the microparticles and microparticle complexes containing insoluble dietary fibers preferably satisfies the specified range. Specifically, the mass ratio of the fine particles and the fine particle composite to the entire composition is usually 4 mass% or more, and among them, preferably 6 mass% or more, more preferably 8 mass% or more, particularly 9 mass% or more, and particularly 10 mass% or more. By setting the mass ratio to the lower limit value or more, the taste of the food containing insoluble dietary fiber can be sufficiently sensed. On the other hand, the upper limit of the above-mentioned mass ratio is usually 98 mass% or less, and among them, 91 mass% or less, further 85 mass% or less, particularly 80 mass% or less, and particularly 55 mass% or less is preferable. By setting the mass ratio to the upper limit value or less, it is possible to easily and preferably ingest the food material containing insoluble dietary fiber. In addition, since the particle complex is a complex of food particles, the taste of food is more easily perceived, and therefore, a complex of food particles containing dietary fiber is preferable.

In the present invention, the content of the microparticles and the microparticle composite in the composition can be performed in the following order, for example. That is, the mass of the components such as food larger than 2000 μm (2mm) which cannot be measured by the laser diffraction particle size distribution measurement or the particle shape image analyzer is removed from the total mass of the insoluble components in the composition is measured. Here, in the case where the composition contains food or the like larger than 2mm, for example, the mass of the precipitated component after separating the supernatant obtained by centrifugal separation is sufficiently removed from the component passing through a 9-mesh sieve (mesh size is 2mm) in the composition is the content of the fine particles and the fine particle composite in the composition (specifically, in the case of solid fat or oil, after removing food or the like larger than 2mm as needed in a state of dissolving by heating, centrifugal separation is performed, and the separation supernatant can be removed). Since a part of the oil and fat or moisture is taken into the precipitation component, the total mass of the fine particles and the fine particle complex in the composition means the total mass of the ingredients and the food materials taken into the precipitation component.

More specifically, in the present invention, the content of the microparticles and the microparticle complex in the composition can be performed in the following order, for example. That is, for example, after passing an arbitrary amount of the composition through a 9-mesh sieve (taylor mesh), the mass of the precipitated component from which the supernatant was separated was sufficiently removed was measured for centrifugal separation at 15000rpm for 1 minute of the passed component, and the content of the microparticles and the microparticle complex in the composition was measured. The residual fraction on the screen when passing through the 9-mesh sieve is obtained by sufficiently passing the insoluble dietary fiber-containing fine particles smaller than the mesh of the 9-mesh sieve through a spatula or the like without changing the particle size of the composition after sufficiently standing. For a composition having a low fluidity to the extent that it does not pass through a 9-mesh sieve (for example, physical properties such as Bostwick viscosity of 10cm or less at 20 ℃ for 30 seconds), the composition may be diluted to about 3 times with a solvent such as olive oil, and the composition passed through a 9-mesh sieve in this state may be centrifuged to measure the content of insoluble dietary fiber-containing microparticles in the composition. The thermoplastic composition may be diluted to about 3 times with a solvent such as water in a heated and fluid state, and the composition passed through a 9-mesh sieve in this state may be centrifuged to measure the content of insoluble dietary fiber-containing microparticles in the composition.

The composition of the present invention preferably contains a predetermined number or more of fine particles or fine particle composites having a particle diameter within a predetermined range before the application of the disturbance, that is, before the ultrasonic treatment. Specifically, the fine particles or fine particle composite to be measured by the particle shape image analyzer having a particle diameter of 2.3 μm to 1600 μm is preferably contained at a concentration of usually 10000 particles/cm³Above, wherein is 10000/cm³Above and further 1000000 pieces/cm³The above. If the content of the fine particles or the fine particle composite having a particle diameter within the above-specified range is less than the above-described lower limit, the effects of the present invention cannot be sufficiently exhibited, which is not preferable. The content number of the fine particles or the fine particle composite having the particle diameter within the above-described predetermined range can be measured by planar particle image analysis (PITA-4) performed by a particle shape analyzer, which is exemplified in the method for analyzing morphological characteristics of particles in the composition.

[ method for producing composition ]

The method for preparing the composition of the present invention is not limited, and any method can be used as long as a composition satisfying the above-described various requirements can be obtained. Specifically, the material of the composition of the present invention, for example, the food material containing insoluble dietary fiber, and other food materials, edible fats and oils, seasonings, and other ingredients that are optionally used may be mixed. However, a method including a step of micronizing an insoluble dietary fiber-containing food material in the presence of an edible oil or fat or other food material or ingredient is preferable. By micronizing the food material containing insoluble dietary fibers in this manner, a complex containing microparticles of insoluble dietary fibers is easily formed. It is not certain why the fine particle composite is formed by such a micronization treatment, but there are possibilities as follows: by micronizing the food material containing insoluble dietary fibers, microparticles containing insoluble dietary fibers are formed, and a plurality of such microparticles are aggregated and reaggregated to form a composite having the above-mentioned specific shape characteristics. The formation of the complex due to such aggregation of the fine particles may be further promoted by, in particular, allowing a certain amount of moisture or fat to coexist, or applying a high shear force, or applying a pressure condition or a temperature-raising condition. Conventionally, it has not been known that under such conditions, a composite having a specific shape characteristic is formed by reaggregation of a particulate composite, or that the above-described various useful effects can be obtained by formation of such a composite.

The method of the micronization treatment used in the present invention is not particularly limited. The temperature for pulverization is not limited, and any of high-temperature pulverization, normal-temperature pulverization, and low-temperature pulverization may be used. The pressure for pulverization is not limited, and any of high-pressure pulverization, normal-pressure pulverization, and low-pressure pulverization may be used. However, from the viewpoint of efficiently obtaining a composition containing microparticles and microparticle complexes having a specific shape defined in the present invention, a method capable of treating food materials and other ingredients as materials of the composition with high shear force under a pressurized condition and a temperature-increasing condition for a short period of time is preferable. Examples of the apparatus used for such a micronization process include: any of machines such as blenders, mixers, mills, kneaders, pulverizers, crushers, and grinders may be used. The system for the pulverization may be either dry pulverization or wet pulverization. In the case of dry pulverization, examples of the device include a media agitation mill such as a dry bead mill and a ball mill (rolling mill, vibration mill, etc.), a jet mill, a high-speed rotary impact mill (pin mill, etc.), a roll mill, a hammer mill, and the like. On the other hand, in the case of wet pulverization, examples of the apparatus include a media agitation mill such as a bead mill or a ball mill (rolling mill, vibration mill, planetary mill, etc.), a roll mill, a colloid mill, Star Burst, and a high-pressure homogenizer. Among them, a medium stirring mill (ball mill, bead mill) or a high-pressure homogenizer is preferable, and a medium stirring mill is more preferable. Among them, a wet media agitation mill, particularly a wet bead mill, is preferably used. By using a wet media agitation mill, it is preferable to use a wet media agitation mill because drying of moisture in the food composition is less likely to occur when the food composition is left standing, and high quality with high stability is obtained, as compared with other micronization treatment methods. The principle is not clear, but is believed to be due to: the fine particle composite in a preferable state is easily formed by the wet medium agitation and grinding treatment.

For example, when the micronization treatment is performed by using a wet media agitation mill such as a wet bead mill, the food material and other components as the material of the composition may be charged into the wet media agitation mill and crushed. The conditions such as the size or filling rate of the beads, the outlet mesh size, the feed rate of the raw material slurry, the rotational strength of the mill, the single pass method (single pass) or the multiple pass method (circulation method), and the like may be appropriately selected and adjusted according to the size or properties of the food material and the properties of the target microparticle complex. Specific conditions are exemplified below, but the present invention is not limited to the following conditions.

The particle size of the beads used in the wet bead mill is usually 2mm or less, preferably 1mm or less. In the case of a bead mill pulverizer using beads having a particle diameter larger than the above upper limit value (for example, a media agitation mill called "ball mill" such as Attritor which generally uses beads having a particle diameter of 3 to 10 mm), it is difficult to pressurize the composition at normal pressure in principle because a long treatment is required to obtain the composition containing the fine particles and the fine particle composite having the specific shape defined in the present invention. The material of the beads used in the wet bead mill is preferably the same as the material of the inner cylinder of the bead mill, and more preferably, the material is zirconia.

The treatment with a wet media agitator mill is preferably carried out under pressure. In order to obtain a satisfactory pressure condition particularly by a bead mill pulverizer, it is preferable to perform the treatment by providing a filter having an appropriate size at the treatment outlet and adjusting the pressure condition while adjusting the liquid feeding speed of the content. The pressure condition at the time of treatment is not limited, and the difference between the maximum pressure during treatment and the normal pressure is usually 0.01MPa or more, preferably 0.02MPa or more, more preferably 0.03Pa or more, and particularly 0.04MPa or more. By setting the difference between the maximum pressure at the time of treatment and the normal pressure to the lower limit value or more, a composition containing the fine particles and the fine particle composite having the specific shape defined in the present invention can be obtained efficiently in a short time. On the other hand, the upper limit of the pressure during the treatment is not limited, but if the pressurization condition is too severe, there is a concern that the equipment may be damaged, and therefore, the difference between the maximum pressure during the treatment and the normal pressure is usually 1MPa or less, and among them, 0.50MPa or less, further 0.40MPa or less, and particularly 0.30MPa or less is preferable.

The temperature at the time of the micronization treatment by the wet media agitation mill is not limited, and any of high-temperature pulverization, normal-temperature pulverization, and low-temperature pulverization may be used. However, it is preferable to adjust the temperature of the sample at the end of the grinding treatment (treatment temperature T)₂) With respect to the sample temperature immediately after the start of the pulverization treatment (treatment temperature: t is₁) Satisfies "T₁+1＜T₂At an elevated temperature in the range of < T1+ 50' (here, the unit is in degrees Celsius (. degree. C.)). The sample temperature at the end of the grinding treatment (treatment temperature: T)₂) Preferably 25 ℃ or higher (T)₂≥25)。

The object of the micronization treatment by the wet media agitation mill is a mixture of the ingredients (insoluble food fiber-containing ingredients and other ingredients) and other ingredients as the material of the composition. It is preferable that such a mixture is subjected to a preliminary treatment such as a coarse pulverization treatment in advance by a jet mill, a pin mill, a stone mill or the like. In this case, it is preferable that the d50 (median particle diameter) of the mixture is adjusted to, for example, a range of usually 10 μm or more, particularly 20 μm or more, and usually 1500 μm or less, particularly 1000 μm or less, and then subjected to the micronization treatment by the media-stirring mill. By adjusting the median particle diameter of the mixture to within this range in advance, it is convenient from the viewpoint of industrial productivity.

In addition, when the mixture to be subjected to the micronization treatment by the wet media agitation and milling contains water, it is preferable to form a state in which the water content of the food materials (insoluble dietary fiber-containing food material and other food materials) is lower than the water content of the other components and the medium, because a composition containing microparticles and microparticle complexes having a specific shape defined in the present invention can be efficiently obtained. Specifically, it is preferable to use dried food materials as food materials (insoluble food fiber-containing food materials and other food materials) and to use water as a medium in addition to oil and fat for the medium agitation grinding treatment, particularly the wet bead mill treatment.

Further, it is preferable to set the viscosity of the mixture to be subjected to the micronization treatment by the wet media agitation mill to a predetermined value or less because a composition containing the fine particles and the fine particle composite having the specific shape defined in the present invention can be efficiently obtained. Specifically, the upper limit of the viscosity (measurement temperature 20 ℃) of the mixture is usually 20 pas or less, and preferably 8 pas or less. On the other hand, the lower limit of the viscosity (measurement temperature 20 ℃) is not particularly limited, but is usually 100 mPas or more, and preferably 500 mPas or more.

Further, if the Bostwick viscosity of the mixture to be subjected to the micronization treatment by the media-agitating mill is adjusted to a predetermined value or less in advance, the pressure at the time of the treatment by the wet media-agitating mill can be easily adjusted to the desired pressure condition, and thus the micronization treatment efficiency is further improved, which is preferable. Specifically, the Bostwick viscosity (measurement temperature 20 ℃) of the mixture is preferably set to usually 28.0cm or less within 1 second.

The number of times and the time of the micronization treatment by the media-stirring mill are not limited, and the pulverization is usually carried out by a single-pass treatment, so that a composition containing the fine particles and the fine particle composite having the specific shape defined in the present invention can be efficiently obtained. In the case of the single pass treatment, the treatment time is preferably 0.1 minute or more, preferably 1 minute or more, more preferably 2 minutes or more, and further preferably 25 minutes or less, preferably 22 minutes or less, more preferably 20 minutes or less. The term "micronization treatment time" used in the medium-stirring mill or the high-pressure homogenizer means a time required for the object to be treated to be sufficiently sheared to form the composition containing the fine particle composite desired in the present invention. As a specific example, when a sample is subjected to a single-pass treatment at a rate of 200mL per minute without circulation using a bead mill crusher having a volume of the pulverization chamber of 100mL and a porosity of 50% after removal of beads (i.e., an injectable treatment solution), the sample treatment time is (100mL × 50%)/(200 mL/min): 0.25 min (15 sec) because the empty volume (empty size) in the pulverization chamber is 50 mL.

[ Properties/uses of the composition ]

The composition of the present invention has various excellent characteristics. One is the increase in emulsification capacity. In the present invention, the "emulsifying capacity" means a mass ratio (%) of the total amount of oil to 1 part by mass of the composition, when salad oil is slowly added while stirring a sample adjusted to 20 ℃ at about 100rpm and oil is added until oil droplets start to float on the surface of the composition. The emulsion capacity was 50% in the case of a total oil charge of 50g relative to 100g of the composition. The composition having a high emulsifying capacity is excellent in the ability to emulsify/stabilize an oil or fat when it is brought into contact with another oil or fat or when it is mixed with another oil or fat. Specifically, the emulsifying capacity of the composition of the present invention is not limited, but is usually 50% or more, preferably 70% or more, more preferably 100% or more, particularly 150% or more, and particularly 200% or more. Due to such characteristics, the composition of the present invention exhibits the following properties: in addition to being useful as a stabilizer for oil-water mixed foods, by eating the composition of the present invention as a food together with a dish containing much oil and fat, drying of the dish (evaporation of water derived from the food material) is prevented, and oil separation of the dish (leaching of oil and fat components derived from the food material) is also suppressed, whereby the taste of the dish can be improved, and this improved taste can be sustained for a long time. In the present specification, unless otherwise specified, "dish containing a large amount of fat" means a dish containing fat in an amount of usually 3% by mass or more, and in particular, 5% by mass or more. Such dishes are available in various forms, and examples thereof include various fried foods.

In addition, the composition of the present invention has a property of reducing (improving) astringency attributable to insoluble dietary fiber when it is eaten as a food. Astringency (Astringent taste, Astringency) refers to a taste that imparts a tight feel to the mouth when the composition is held in the mouth. The mechanism of its production is not clear, but it is considered that astringency is different from a taste felt by stimulating nerve cells of taste, which is a sensation similar to a sense of touch felt by contracting cells in the mouth. For example, red wine is characterized by astringent taste derived from tannin derived from grape, which is similar to astringent (astringent), bitter or pungent taste (えぐみ), but is perceived differently. This astringency is usually present in food products containing insoluble dietary fibers, and thus tends to be an obstacle to eating. However, the composition of the present invention contains insoluble dietary fiber, but is easy to eat because of reduced astringency. The principle of this improvement in astringency is not clear, but the following possibilities are considered: as the emulsifying capacity of the composition increases, its affinity for lipids increases, thereby having a slight effect on lipid membranes on the surface of taste bud cells.

The composition of the present invention may have excellent stability such as water separation resistance (property of inhibiting water separation) and drying resistance (property of inhibiting drying due to water evaporation). Because of such excellent stability, the composition of the present invention is advantageous because the risk of microbial growth, flavor deterioration, and the like is reduced when the composition is distributed as a food product on a commercial basis.

The composition of the present invention can be directly eaten as a food in this state, and can be suitably used as a raw material or a raw material for a food or drink or a liquid seasoning. That is, the present invention is directed to foods, drinks and liquid seasonings containing the composition of the present invention. By using the composition of the present invention as a part of the raw material, seasonings such as sauces, dips, mayonnaises, dressings, butters, and jams having high dispersion stability can be produced. When the composition of the present invention is added to a seasoning in this manner, the amount of the composition of the present invention added to the seasoning is not limited, and is preferably about 0.001 to 50% by mass. In addition, the composition may be added to the seasoning at any time during the production. Specifically, the composition may be added to a seasoning, or a material (food material or the like) of the composition of the present invention may be added to a raw material of a seasoning and then subjected to a micronization treatment, or these methods may be combined, and a method of adding the composition of the present invention to a seasoning is industrially convenient and preferable. The composition of the present invention is expected to be applied mainly in the field of foods because of the above-mentioned unknown property of reducing astringency. In addition, due to the above-mentioned unknown property of improved emulsifying capacity, it is possible to use as an alternative to an emulsifier mainly in industries avoiding the use of food additives, such as bread manufacturing industry, even in the food field. The composition of the present invention is industrially advantageous because it can be widely used in various fields as a substitute for an emulsifier in addition to the food field due to the unknown property of improving the emulsifying capacity.

In addition, if the effect of improving the emulsifying capacity, which is an unknown property exhibited by the composition of the present invention, is applied, a method of improving the emulsifying capacity of a composition containing insoluble dietary fibers is also proposed as one aspect of the present invention. This method of increasing the emulsifying capacity comprises: any composition comprising insoluble dietary fibres is converted into the above-described composition of the invention by subjecting it to a comminuting treatment. In this method for improving the emulsifying capacity, the composition containing insoluble dietary fibers corresponds to a mixture of the food material and other ingredients which are the components of the composition of the present invention and are to be micronized by the above-described method for producing the composition of the present invention. For further details, the compositions of the invention and methods of making the same are described previously.

In addition, if the effect of improving (reducing) astringency, which is an unknown attribute exhibited by the composition of the present invention, is applied, as one aspect of the present invention, a method of improving astringency of a composition containing insoluble dietary fiber is also proposed. The method for improving astringency comprises: any composition comprising insoluble dietary fibres is converted into the above-described composition of the invention by subjecting it to a comminuting treatment. In this method for improving astringency, the composition containing insoluble dietary fibers corresponds to a mixture of food materials and other ingredients that are constituents of the composition of the present invention and are to be micronized in the above-described method for producing the composition of the present invention. For further details, the compositions of the invention and methods of making the same are described previously.

Examples

The present invention will be described in further detail with reference to examples below, which are provided for convenience of explanation and are not to be construed as limiting the scope of the present invention in any way.

[ preparation of sample composition ]

The composition samples of test examples 1 to 41 were prepared as follows.

Dried products of apples and avocados, which are one kind of fruits, kelp, which is one kind of algae, cashews, which are one kind of seeds, corns, which are one kind of grains, and beets, carrots, pumpkins, peppers, broccoli, and tomatoes, which are one kind of vegetables, were pulverized according to the method described in "pretreatment" of table 3 below, and dried and pulverized products were obtained. In addition, green peas, soybeans, and green beans (beans obtained by harvesting soybeans together with pods in an immature state and having green appearance) which are one kind of beans were boiled, and dried and taken out from the pods, and the dried products were pulverized as edible parts according to the method described in "pretreatment" in table 3 below, to obtain dry pulverized products. All the dry pulverized products are subjected to a drying treatment until the water activity is at least 0.95 or less. Note that, a part normally subjected to diet (a part other than the inedible part) is used as the edible part of each food material, and the corn core, the pepper seed or stalk, the pumpkin seed or pulp, the beet peel, the broccoli stem and leaf, the green soy bean pod, and the tomato stalk are used as the inedible part of some food materials.

According to the formulation shown in the following table, these dry pulverized materials were appropriately mixed together with water as a medium and optional fats and oils, and sufficiently stirred with a desk mixer until the appearance was substantially uniform, to obtain a paste-like coarsely pulverized composition. As the fat and oil, commercially available olive oil (saturated fatty acid: 14%, unsaturated fatty acid: 80%) was used.

These coarsely pulverized compositions were optionally pretreated in accordance with the method described in "pretreatment" of table 3 below, and then subjected to micronization treatment in accordance with the method described in "micronization treatment method" of table 3 below. In the case of using "beads" as a medium, each composition sample was obtained by performing a micronization treatment using a wet bead mill and beads having a diameter of 1mm under the treatment conditions described in the following table. The pressure conditions were adjusted by appropriately changing the mesh size of the outlet of the wet bead mill and the liquid feeding speed so that the maximum pressure during the treatment (pressure 0, since the pressure is not increased in the case of the treatment under normal pressure) reached the pressure conditions shown in the following table, and the fine treatment was performed under a certain condition until the end of the treatment.

[ analysis of characteristics relating to morphology and physical Properties of composition samples ]

The composition samples of test examples 1 to 41 obtained in the above-described order were analyzed for their morphological and physical properties in the following order.

< morphological characteristics analysis (major axis, minor axis, concavity and convexity) of a sample of the composition >

In morphological feature analysis of particles (fine particles and fine particle composites) in each composition sample (before ultrasonic treatment) in a state where no disturbance was applied, PITA-4 manufactured by Seishin corporation was used as a particle analyzer of a particle analysis type by a dynamic image analysis method and capable of being provided with a high-pixel camera described later. In The case of taking a particle image, DMK33UX290 (manufactured by The Imaging Source) is used as a camera capable of taking a planar image having an effective pixel number of 1920(H) × 1080(V) and a pixel size of about 2.8 μm × 2.8 μm in more detail. As an objective lens for photographing, an objective lens of 4 times magnification was used, and as a flow cell, a plane expansion cell made of synthetic quartz glass was used.

The images of the particles in each composition sample were taken by diluting each composition sample to 1000-fold with a solvent and flowing the diluted composition sample into a flow cell at an appropriate flow rate. When a particle image is captured, conditions of a particle image analyzer are set so as to be focusedThe particle shape in the sample can be clearly confirmed by setting the dot appropriately, and the particle in the sample can be clearly discriminated by setting the contrast with the background appropriately. As an example of setting analysis conditions for acquiring a particle image, a planar image is acquired as an LED intensity of 100 and a camera gain of 100db using an 8-Bit-gradation camera, and then 10000 or more images of each particle are captured and subjected to morphological feature analysis with the brightness level of the particle image existing therein set to 115 and the contour level set to 160. Distilled water was used as a solvent and a carrier liquid for the measurement. Note that all 1cm before the ultrasonic treatment was used³At least 10000 particles having a particle diameter of 2.3 to 1600 μm were confirmed in the composition sample.

In 10000 particle images (pixel size 2.8 μm × 2.8 μm) of 1920 pixels × 1080 pixels obtained by imaging each composition sample before the ultrasonic treatment, the "major axis" and the "minor axis" and the "roughness" of the particles having the lowest number of pixels of 15 pixels or more were measured by the above method, and the above numerical values n (i) to n (iii) were calculated. In calculating the numerical value n (iii), the specific surface area per unit volume after the ultrasonic treatment described later is also used.

< particle size distribution (mode diameter, maximum particle diameter, d50, specific surface area per unit volume) >)

The particle size distribution of each composition sample was measured using a Microtrac MT3300 EX2 system, manufactured by Microtrac bel co. Distilled water was used as a solvent for measurement, and DMSII (Data Management System version2, MicrotracBEL corporation) was used as measurement application software. During measurement, after a washing button of measurement application software is pressed to wash, a Setzero button of the software is pressed to perform zero adjustment, and a sample is directly put into the device by using sample loading until a proper concentration range is reached.

In the measurement of a sample without disturbance, that is, a sample before ultrasonic treatment, the sample concentration was adjusted to an appropriate range within 2 sample loads after the sample was put in, and immediately thereafter, laser diffraction measurement was performed at a flow rate of 60% for a measurement time of 10 seconds, and the obtained result was used as a measurement value. On the other hand, in the measurement of a sample subjected to disturbance, that is, a sample after ultrasonic treatment, the sample concentration is adjusted to an appropriate range by sample loading after the sample is put in, and then an ultrasonic treatment button of the software is pressed to output 40W and ultrasonic waves having a frequency of 40kHz are applied for 3 minutes. After that, after 3 times of defoaming treatment and sample loading treatment again, it was confirmed that the sample concentration was still in an appropriate range, laser diffraction measurement was rapidly performed at a flow rate of 60% for a measurement time of 10 seconds, and the obtained result was used as a measurement value. As the measurement conditions, the following conditions were employed: and (3) distribution display: volume, particle refractive index: 1.60, solvent refractive index: 1.333, 2000.00 μm as an upper limit of measurement (μm), and 0.021 μm as a lower limit of measurement (μm).

In the measurement of the particle size distribution of each channel of the sample, the measurement was performed using the particle size of each measurement channel described in the following table 2 as a standard. The frequency of particles having a particle diameter not larger than the predetermined particle diameter of each channel and larger than the predetermined particle diameter of the next channel (the lower measurement limit particle diameter in the maximum channel of the measurement range) is measured for each channel, and the frequency% of particles in each channel is obtained by using the total frequency of all channels in the measurement range as a denominator. Specifically, the following 132 channels were measured for each of the% particle frequency. The particle diameter of the channel having the largest particle frequency% was regarded as the mode particle diameter in the measurement results. In the case where there are a plurality of channels having the same particle frequency%, the particle diameter of the channel in which the particle diameter is smallest is adopted as the mode particle diameter. In addition, among the channels in which the particle frequency was confirmed, the channel having the largest particle size was used as the maximum particle size.

[ Table 2]

Channel	Particle size (. mu.m)	Channel	Particle size (. mu.m)	Channel	Particle size (. mu.m)	Channel	Particle size (. mu.m)
								1	2000.000	37	88.000	73	3.889	109	0.172
2	1826.000	38	80.700	74	3.566	110	0.158
								3	1674.000	39	74.000	75	3.270	111	0.145
4	1535.000	40	67.860	76	2.999	112	0.133
								5	1408.000	41	62.230	77	2.750	113	0.122
6	1291.000	42	57.060	78	2.522	114	0.111
								7	1184.000	43	52.330	79	2.312	115	0.102
8	1086.000	44	47.980	80	2.121	116	0.094
								9	995.600	45	44.000	81	1.945	117	0.086
10	913.000	46	40.350	82	1.783	118	0.079
								11	837.200	47	37.000	83	1.635	119	0.072
12	767.700	48	33.930	84	1.499	120	0.066
								13	704.000	49	31.110	85	1.375	121	0.061
14	645.600	50	28.530	86	1.261	122	0.056
								15	592.000	51	26.160	87	1.156	123	0.051
16	542.900	52	23.990	88	1.060	124	0.047
								17	497.800	53	22.000	89	0.972	125	0.043
18	456.500	54	20.170	90	0.892	126	0.039
								19	418.600	55	18.500	91	0.818	127	0.036
20	383.900	56	16.960	92	0.750	128	0.033
								21	352.000	57	15.560	93	0.688	129	0.030
22	322.800	58	14.270	94	0.630	130	0.028
								23	296.000	59	13.080	95	0.578	131	0.026
24	271.400	60	12.000	96	0.530	132	0.023
								25	248.900	61	11.000	97	0.486
26	228.200	62	10.090	98	0.446
								27	209.300	63	9.250	99	0.409
28	191.900	64	8.482	100	0.375
								29	176.000	65	7.778	101	0.344
30	161.400	66	7.133	102	0.315
								31	148.000	67	6.541	103	0.289
32	135.700	68	5.998	104	0.265
								33	124.500	69	5.500	105	0.243
34	114.100	70	5.044	106	0.223
								35	104.700	71	4.625	107	0.204
36	95.960	72	4.241	108	0.187

< emulsion Capacity >

Each composition sample was adjusted to 20 ℃ and salad oil was slowly injected while stirring at about 100rpm, the injection was stopped at the time point when the oil droplets started to float on the surface of the composition, and the mass ratio (%) of the total amount of oil injected to the composition sample was determined.

[ sensory evaluation of composition samples ]

The sensory evaluation was performed on the composition samples of test examples 1 to 41 obtained in the above-described procedure in the following manner.

< inhibition of drying, inhibition of oil separation and taste of oil-and fat-containing dishes >

Fried chicken (lipid 8%) was used as the oil-and-lipid dish. After heating the dish, a 1-spoon sample of each composition was placed on it and allowed to stand overnight (approximately 16 hours) in a refrigerator (4 ℃). Then, 10 trained sensory examiners in total tried the dishes to evaluate the quality of taste upon eating.

Specifically, regarding "drying inhibition", the degree of dryness of dishes upon eating was evaluated on the following 5-degree scale. 5: the product is moist and delicious; 4: slightly moist and slightly delicious; 3: slightly dry, but within acceptable ranges; 2: slightly dry, not delicious; 1: dried and crispy, and not delicious.

In addition, regarding "oil separation suppression", oil separation from dishes (extraction of oil and fat components derived from food materials) at the time of eating was evaluated on the following 5 ranks. 5: less oil separation; 4: slightly less oil separation; 3: with oil separation, but within acceptable limits; 2: slightly more oil-off; 1: much oil is separated.

In addition, regarding "taste of the oil and fat-containing dish", the taste of the oil and fat-containing dish (fried chicken) was evaluated on the following 5 grades. 5: the taste is good; 4: is slightly delicious; 3: common; 2: slightly delicious; 1: it is not delicious.

< astringent taste >

A total of 10 trained sensory examiners tried 1 tablespoon of each composition sample and evaluated the quality of "astringency" upon eating. Specifically, the astringency of the composition samples upon consumption was evaluated on the following 5-point scale. 5: has no astringent taste and good taste; 4: the astringent taste is less and the taste is slightly delicious; 3: slightly astringent, but within acceptable ranges; 2: the astringent taste is slightly obvious and slightly delicious; 1: has obvious astringent taste and is not delicious.

< stability (anti-dehydration), stability (anti-drying) >

Each composition sample was thinly spread in a pan with a thickness of 1mm, and visually observed by 10 trained sensory inspectors in total, and the quality thereof was evaluated.

Specifically, with respect to "stability (prevention of water separation)", the degree of separation of water from a composition sample left standing overnight (16 hours) at 4 ℃ was evaluated by a sensory inspector as compared with a composition sample immediately after production. As the score, evaluation was performed on the following 5 ranks. 5: little water, preferably; 4: droplet separation was confirmed on the surface of the composition, but overall less, slightly preferred; 3: droplet separation was confirmed on the surface of the composition, but within an acceptable range; 2: droplet separation was confirmed on the surface of the composition, which was slightly more numerous and slightly less preferred; 1: droplet separation was confirmed on the surface of the composition, and the amount thereof was significant, not preferable.

In addition, regarding "stability (anti-drying)", the degree of drying of the composition sample left standing overnight (16 hours) at 4 ℃ was evaluated by a sensory inspector as compared with the composition sample immediately after the production. As the score, evaluation was performed on the following 5 ranks. 5: less drying of the composition, preferably; 4: the drying of the composition is slightly less, slightly preferred; 3: the composition is dry but within acceptable limits; 2: drying of the composition is slightly apparent, slightly less preferred; 1: drying of the composition is apparent and not preferred.

< sensory evaluation order of execution >

In each of the above sensory tests, the following recognition training a) to C) was performed on sensory examiners regarding evaluation items related to taste, i.e., "drying suppression", "oil separation suppression", "taste of oil-and fat-containing dishes", and then, examiners having particularly excellent performance, having good experience in developing products, having rich knowledge on qualities such as taste and appearance of foods, and being able to perform absolute evaluation on each sensory examination item were selected.

A) Taste quality identification test: for five flavors (sweet taste: sugar taste; sour taste: tartaric acid taste; umami taste: sodium glutamate taste; salty taste: sodium chloride taste; bitter taste: caffeine taste), 1 part each of aqueous solutions having concentrations close to the threshold value of each component was prepared, and 2 parts of distilled water was added thereto, and samples of each taste were accurately identified from 7 total samples.

B) Concentration difference identification test: accurately identifying the concentration difference of 5 kinds of saline solution and acetic acid aqueous solution with slightly different concentrations;

C)3, point identification test: the soy sauce of company B was accurately identified from a total of 3 samples of 2 soy sauce of company a and 1 soy sauce of company B.

In all of the above evaluation items, the whole examiner previously evaluated the standard sample, normalized each score of the evaluation criteria, and then subjected to objective sensory examination by 10 persons in total. The evaluation of each evaluation item was performed such that each examiner selects any one of the 5-level scores of each item, which is the closest to his/her own evaluation. The statistics of the evaluation results were calculated from the arithmetic mean of the scores of 10 in total, and the standard deviation was calculated in order to further evaluate the difference between the sensory examiners.

[ analysis/evaluation results of composition sample ]

The analysis and evaluation results of the composition samples of test examples 1 to 41 are shown in Table 3 below.

[ Table 3-1]

[ tables 3-2]

[ tables 3 to 3]

[ tables 3 to 4]

[ tables 3 to 5]

[ tables 3 to 6]

[ tables 3 to 7]

[ tables 3 to 8]

[ tables 3 to 9]

[ tables 3 to 10]

[ Table 4-1]

[ tables 4-2]

[ tables 4 to 3]

[ tables 4 to 4]

[ tables 4 to 5]

[ tables 4 to 6]

[ tables 4 to 7]

[ tables 4 to 8]

[ tables 4 to 9]

[ tables 4 to 10]

Industrial applicability

The composition of the present invention is expected to be applied mainly to the food field due to the above-mentioned unknown property of reducing astringency, and is industrially advantageous because it is widely used as a substitute for an emulsifier in various fields other than the food field due to the above-mentioned unknown property of improving an emulsifying capacity.

Claims

1. A composition containing a microparticle complex comprising insoluble dietary fibers, which satisfies the following (1) to (5) and at the same time satisfies one or more of the following (6-1) to (6-3):

(1) contains 0.1 mass% or more of insoluble dietary fiber;

(2) the total oil content is less than 20 mass percent;

(3) the maximum grain size before ultrasonic treatment is more than 100 mu m;

(4) the mode diameter before ultrasonic treatment is 5-400 [ mu ] m;

(6-1) the value N (I) obtained by the following formula (I) is 1.20 or more;

(math formula 1)

N(I)=(α/β)　　　(I)

(6-2) the value N (II) obtained by the following formula (II) is 1.40 or more;

(math figure 2)

N(II)=(α/β)/ω　 (II)

(math figure 3)

N(III)=(α/β)×γ_A　　(III)

Wherein, in the above formulas (I) to (III),

2. The composition according to claim 1, wherein the water content/(water content + total oil component content) is 75% or more.

3. The composition of claim 1 or 2, wherein the specific surface area per unit volume (γ) before ultrasonication is_B) Specific surface area per unit volume (gamma) after ultrasonic treatment_A) Ratio of (gamma)_B/γ_A) Is 0.8 or less.

4. The composition according to any one of claims 1 to 3, which has an emulsifying capacity of 50% or more.

5. The composition according to any one of claims 1 to 4, wherein the content of the microparticle complex is 4% by mass or more and 98% by mass or less.

6. The composition of any one of claims 1 to 5, wherein the insoluble dietary fiber comprises dietary fiber from the edible part and/or the non-edible part of a food material comprising insoluble dietary fiber.

7. The composition of claim 6, wherein the insoluble dietary fiber comprises dietary fiber from the edible portion and the non-edible portion of the same class of food material comprising insoluble dietary fiber.

8. The composition according to claim 6 or 7, wherein the insoluble food fiber-containing food material is one or more selected from the group consisting of seeds, grains, beans, vegetables and fruits.

9. The composition according to claim 8, wherein the food material containing insoluble dietary fiber is one or more selected from carrot, pumpkin, corn, soybean, green soy bean, chili pepper, beet, green pea, broccoli and tomato.

10. The composition according to claim 9, wherein the non-edible part of the food material containing insoluble dietary fiber is at least one selected from the group consisting of a core of sweet corn, a seed or stalk of hot pepper, a seed or flesh of pumpkin, a skin of beet, a stem and leaf of broccoli, a pod of green soybean, and a stalk of tomato.

11. The composition as claimed in any one of claims 6 to 10, which comprises a pulverized material of food material containing insoluble dietary fiber.

12. The composition according to claim 11, wherein the pulverization treatment product is a medium-stirring mill treatment product.

13. The composition according to claim 12, wherein the media-agitating mill treatment is a wet media-agitating mill treatment.

14. The composition according to any one of claims 11 to 13, which satisfies one or more of the following (6-1 ') to (6-3'):

(6-1') in a state where the grinding treatment is carried out until the value N (I) obtained by the above formula (I) is increased by 5% or more before and after the grinding;

(6-2') in a state where the grinding treatment is carried out until the value N (II) obtained by the above formula (II) is increased by 5% or more before and after the grinding;

(6-3') is a state in which the pulverization treatment is carried out until the numerical value N (III) obtained by the above formula (III) is increased by 5% or more before and after the pulverization.

15. A food or beverage comprising the composition according to any one of claims 1 to 14.

16. A liquid seasoning comprising the composition according to any one of claims 1 to 14.

17. A method of making the composition of any one of claims 1 to 14, the method comprising: the food material containing insoluble dietary fiber is pulverized.

18. The method of claim 16 or 17, wherein the pulverizing process is a media-agitating mill process.

19. The method of claim 18, wherein the comminution process is a wet media agitator mill process.

20. The method according to any one of claims 17 to 19, wherein the media-agitating mill treatment is performed under a pressure condition in which a maximum pressure is 0.01MPa or more and 1MPa or less.

21. The method of any one of claims 17 to 20, wherein the media-agitating mill treatment is at a treatment temperature T at the start of the treatment₁(. degree. C.) and the treatment temperature at the end, T₂(DEG C) under a temperature-raising condition satisfying the following formula (A):

(math figure 4)

T₁+1＜T₂＜T₁+50　　　　(A)。

22. The method according to any one of claims 17 to 21, wherein the water activity value of the insoluble dietary fiber-containing food material is 0.95 or less.

23. The method according to any one of claims 17 to 22, wherein the amount of available carbohydrate in the insoluble dietary fiber-containing material is 2% by mass or more.

24. A method of increasing the emulsification capacity of a composition comprising insoluble dietary fiber, the method comprising: forming the composition of any one of claims 1 to 14 by subjecting a composition comprising insoluble dietary fibres to a size reduction treatment.

25. A method of improving the astringency of a composition comprising insoluble dietary fiber, the method comprising: forming the composition of any one of claims 1 to 14 by subjecting a composition comprising insoluble dietary fibres to a size reduction treatment.

26. A method for producing a liquid seasoning by containing the composition according to any one of claims 1 to 14.

27. The method according to any one of claims 17 to 26, wherein the pulverization treatment is performed until one or more of the following (6-1 ') to (6-3') are satisfied: